Organometallic compound, organic light-emitting device including the organometallic compound, and diagnostic compositions including the organometallic compound

ABSTRACT

An organometallic compound represented by Formula 1: 
                         
wherein in Formula 1, groups and variables are the same as described in the specification.

CROSS-REFERENCE TO RELATED APPLICATION

This application claims priority to Korean Patent Application No. 10-2017-0027772, filed on Mar. 3, 2017, in the Korean Intellectual Property Office, and all the benefits accruing therefrom under 35 U.S.C. § 119, the content of which is incorporated herein in its entirety by reference.

BACKGROUND 1. Field

One or more embodiments relate to an organometallic compound, an organic light-emitting device including the organometallic compound, and a diagnostic composition including the organometallic compound.

2. Description of the Related Art

Organic light-emitting devices (OLEDs) are self-emission devices, which have superior characteristics in terms of a viewing angle, a response time, a brightness, a driving voltage, and a response speed, and which produce full-color images.

A typical organic light-emitting device includes an anode, a cathode, and an organic layer disposed between the anode and the cathode, wherein the organic layer includes an emission layer. A hole transport region may be disposed between the anode and the emission layer, and an electron transport region may be disposed between the emission layer and the cathode. Holes provided from the anode may move toward the emission layer through the hole transport region, and electrons provided from the cathode may move toward the emission layer through the electron transport region. The holes and the electrons recombine in the emission layer to produce excitons. These excitons transit from an excited state to a ground state, thereby generating light.

Meanwhile, luminescent compounds may be used to monitor, sense, or detect a variety of biological materials including cells and proteins. An example of the luminescent compounds includes a phosphorescent luminescent compound.

Various types of organic light emitting devices are known. However, there still remains a need in OLEDs having low driving voltage, high efficiency, high brightness, and long lifespan.

SUMMARY

One or more embodiments include an organometallic compound, an organic light-emitting device including the organometallic compound, and a diagnostic composition including the organometallic compound.

Additional aspects will be set forth in part in the description which follows and, in part, will be apparent from the description, or may be learned by practice of the presented embodiments.

According to one or more embodiments, an organometallic compound is represented by Formula 1:

In Formulae 1, CZ1, CZ3, and CZ4,

-   -   M may be selected from a first-row transition metal of the         Periodic Table of Elements, a second-row transition metal of the         Periodic Table of Elements, and a third-row transition metal of         the Periodic Table of Elements,     -   X₁ to X₄ may each independently be C or N,     -   two bonds selected from a bond between X₁ and M, a bond between         X₂ and M, a bond between X₃ and M, and a bond between X₄ and M         may each be a coordinate bond, and the others thereof may each         be a covalent bond,     -   Y₂ to Y₅ may each independently be C or N,     -   Y₁ and Y₆ may each independently be C, N, O, Si, or S,     -   a bond between X₁ and Y₁, a bond between X₁ and Y₂, a bond         between X₃ and Y₃, a bond between X₃ and Y₄, a bond between X₄         and Y₅, and a bond between X₄ and Y₆ may each be a chemical bond         that links the corresponding atoms,     -   CY₁ may be selected from a C₅-C₃₀ carbocyclic group, a C₁-C₃₀         heterocyclic group, and a group represented by Formula CZ1,     -   CY₃ may be selected from a C₅-C₃₀ carbocyclic group, a C₁-C₃₀         heterocyclic group, and a group represented by Formula CZ3,     -   CY₄ may be selected from a C₅-C₃₀ carbocyclic group, a C₁-C₃₀         heterocyclic group, and a group represented by Formula CZ4,     -   T₁ to T₃ may each independently be selected from         *—N[(L₅)_(b5)-(R₅)]—*′, *—B(R₅)—*′, *—P(R₅)—*′, *—C(R₅)(R₆)—*′,         *—Si(R₅)(R₆)—*′, *—Ge(R₅)(R₆)—*′, *—S—*′, *—Se—*′, *—O—*′,         *—C(═O)—*′, *—S(═O)—*′, *—S(═O)₂—*′, *—C(R₅)═*′, *═C(R₅)—*′,         *—C(R₅)═C(R₆)—*′, *—C(═S)—*′, and *—C≡C—*′,     -   L₅ may be selected from a single bond, a substituted or         unsubstituted C₅-C₃₀ carbocyclic group, and a substituted or         unsubstituted C₁-C₃₀ heterocyclic group,     -   b5 may be selected from 1 to 3, wherein, when b5 is two or more,         two or more groups L₅ may be identical to or different from each         other,     -   R₅ and R₆ may optionally be linked via a first linking group to         form a substituted or unsubstituted C₅-C₃₀ carbocyclic group or         a substituted or unsubstituted C₁-C₃₀ heterocyclic group,     -   n1 to n3 may each independently be 0, 1, 2, or 3, wherein, when         n1 is zero, *-(T₁)_(n1)-*′ may be a single bond, when n2 is         zero, *-(T₂)_(n2)-*′ may be a single bond, and when n3 is zero,         *-(T₃)_(n3)-*′ may be a single bond,

X₁₁ may be N or C(R₁₁), X₁₂ may be N or C(R₁₂), X₁₃ may be N or C(R₁₃), X₁₄ may be N or C(R₁₄), X₁₅ may be N or C(R₁₅), X₁₆ may be N or C(R₁₆), X₁₇ may be N or C(R₁₇), X₂₁ may be N or C(R₂₁), X₂₂ may be N or C(R₂₂), X₂₃ may be N or C(R₂₃), X₂₄ may be N or C(R₂₄), X₂₅ may be N or C(R₂₅), X₂₆ may be N or C(R₂₆), X₃₁ may be N or C(R₃₁), X₃₂ may be N or C(R₃₂), X₃₃ may be N or C(R₃₃), X₃₄ may be N or C(R₃₄), X₃₅ may be N or C(R₃₅), X₃₆ may be N or C(R₃₆), X₄₁ may be N or C(R₄₁), X₄₂ may be N or C(R₄₂), X₄₃ may be N or C(R₄₃), X₄₄ may be N or C(R₄₄), X₄₅ may be N or C(R₄₅), X₄₆ may be N or C(R₄₆), and X₄₇ may be N or C(R₄₇),

-   -   R₁, R₃ to R₆, R₁₁ to R₁₇, R₂₁ to R₂₆, R₃₁ to R₃₆, and R₄₁ to R₄₇         may each independently be selected from hydrogen, deuterium, —F,         —Cl, —Br, —I, —SF₅, a hydroxyl group, a cyano group, a nitro         group, an amidino group, a hydrazine group, a hydrazone group, a         carboxylic acid group or a salt thereof, a sulfonic acid group         or a salt thereof, a phosphoric acid group or a salt thereof, a         substituted or unsubstituted C₁-C₆₀ alkyl group, a substituted         or unsubstituted C₂-C₆₀ alkenyl group, a substituted or         unsubstituted C₂-C₆₀ alkynyl group, a substituted or         unsubstituted C₁-C₆₀ alkoxy group, a substituted or         unsubstituted C₃-C₁₀ cycloalkyl group, a substituted or         unsubstituted C₁-C₁₀ heterocycloalkyl group, a substituted or         unsubstituted C₃-C₁₀ cycloalkenyl group, a substituted or         unsubstituted C₁-C₁₀ heterocycloalkenyl group, a substituted or         unsubstituted C₆-C₆₀ aryl group, a substituted or unsubstituted         C₆-C₆₀ aryloxy group, a substituted or unsubstituted C₆-C₆₀         arylthio group, a substituted or unsubstituted C₇-C₆₀ arylalkyl         group, a substituted or unsubstituted C₁-C₆₀ heteroaryl group, a         substituted or unsubstituted C₁-C₆₀ heteroaryloxy group, a         substituted or unsubstituted C₁-C₆₀ heteroarylthio group, a         substituted or unsubstituted C₂-C₆₀ heteroarylalkyl group, a         substituted or unsubstituted monovalent non-aromatic condensed         polycyclic group, a substituted or unsubstituted monovalent         non-aromatic condensed heteropolycyclic group, —N(Q₁)(Q₂),         —Si(Q₃)(Q₄)(Q₅), —B(Q₆)(Q₇), and —P(═O)(Q₈)(Q₉),     -   a1, a3, and a4 may each independently be 0, 1, 2, 3, 4, or 5,     -   two of groups R₁ in the number of a1 may optionally be linked to         form a substituted or unsubstituted C₅-C₃₀ carbocyclic group or         a substituted or unsubstituted C₁-C₃₀ heterocyclic group,     -   two of groups R₃ in the number of a3 may optionally be linked to         form a substituted or unsubstituted C₅-C₃₀ carbocyclic group or         a substituted or unsubstituted C₁-C₃₀ heterocyclic group,     -   two of groups R₄ in the number of a4 may optionally be linked to         form a substituted or unsubstituted C₅-C₃₀ carbocyclic group or         a substituted or unsubstituted C₁-C₃₀ heterocyclic group,     -   two of R₁₁ to R₁₇ may optionally be linked to form a substituted         or unsubstituted C₅-C₃₀ carbocyclic group or a substituted or         unsubstituted C₁-C₃₀ heterocyclic group,     -   two of R₂₁ to R₂₆ may optionally be linked to form a substituted         or unsubstituted C₅-C₃₀ carbocyclic group or a substituted or         unsubstituted C₁-C₃₀ heterocyclic group,     -   two of R₃₁ to R₃₆ may optionally be linked to form a substituted         or unsubstituted C₅-C₃₀ carbocyclic group or a substituted or         unsubstituted C₁-C₃₀ heterocyclic group,     -   two of R₄₁ to R₄₇ may optionally be linked to form a substituted         or unsubstituted C₅-C₃₀ carbocyclic group or a substituted or         unsubstituted C₁-C₃₀ heterocyclic group,     -   *, *′, and *″ each indicate a binding site to a neighboring         atom,     -   at least one substituent of the substituted C₅-C₃₀ carbocyclic         group, the substituted C₁-C₃₀ heterocyclic group, the         substituted C₁-C₆₀ alkyl group, the substituted C₂-C₆₀ alkenyl         group, the substituted C₂-C₆₀ alkynyl group, the substituted         C₁-C₆₀ alkoxy group, the substituted C₃-C₁₀ cycloalkyl group,         the substituted C₁-C₁₀ heterocycloalkyl group, the substituted         C₃-C₁₀ cycloalkenyl group, the substituted C₁-C₁₀         heterocycloalkenyl group, the substituted C₆-C₆₀ aryl group, the         substituted C₆-C₆₀ aryloxy group, the substituted C₆-C₆₀         arylthio group, the substituted C₇-C₆₀ arylalkyl group, the         substituted C₁-C₆₀ heteroaryl group, the substituted C₁-C₆₀         heteroaryloxy group, the substituted C₁-C₆₀ heteroarylthio         group, the substituted C₂-C₆₀ heteroarylalkyl group, the         substituted monovalent non-aromatic condensed polycyclic group,         and the substituted monovalent non-aromatic condensed         heteropolycyclic group may be selected from:     -   deuterium, —F, Cl, —Br, —I, —CD₃, —CD₂H, —CDH₂, a hydroxyl         group, a cyano group, a nitro group, an amidino group, a         hydrazine group, a hydrazone group, a carboxylic acid group or a         salt thereof, a sulfonic acid group or a salt thereof, a         phosphoric acid group or a salt thereof, a C₁-C₆₀ alkyl group, a         C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl group, and a C₁-C₆₀         alkoxy group;     -   a C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl         group, and a C₁-C₆₀ alkoxy group, each substituted with at least         one selected from deuterium, —F, —Cl, —Br, —I, —CD₃, —CD₂H,         —CDH₂, a hydroxyl group, a cyano group, a nitro group, an         amidino group, a hydrazine group, a hydrazone group, a         carboxylic acid group or a salt thereof, a sulfonic acid group         or a salt thereof, a phosphoric acid group or a salt thereof, a         C₃-C₁₀ cycloalkyl group, a C₁-C₁₀ heterocycloalkyl group, a         C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀ heterocycloalkenyl group, a         C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio         group, a C₇-C₆₀ arylalkyl group, a C₁-C₆₀ heteroaryl group, a         C₁-C₆₀ heteroaryloxy group, a C₁-C₆₀ heteroarylthio group, a         C₂-C₆₀ heteroarylalkyl group, a monovalent non-aromatic         condensed polycyclic group, a monovalent non-aromatic condensed         heteropolycyclic group, —N(Q₁₁)(Q₁₂), —Si(Q₁₃)(Q₁₄)(Q₁₅),         —B(Q₁₆)(Q₁₇), and —P(═O)(Q₁₈)(Q₁₉);     -   a C₃-C₁₀ cycloalkyl group, a C₁-C₁₀ heterocycloalkyl group, a         C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀ heterocycloalkenyl group, a         C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio         group, a C₇-C₆₀ arylalkyl group, a C₁-C₆₀ heteroaryl group, a         C₁-C₆₀ heteroaryloxy group, a C₁-C₆₀ heteroarylthio group, a         C₂-C₆₀ heteroarylalkyl group, a monovalent non-aromatic         condensed polycyclic group, and a monovalent non-aromatic         condensed heteropolycyclic group;     -   a C₃-C₁₀ cycloalkyl group, a C₁-C₁₀ heterocycloalkyl group, a         C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀ heterocycloalkenyl group, a         C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio         group, a C₇-C₆₀ arylalkyl group, a C₁-C₆₀ heteroaryl group, a         C₁-C₆₀ heteroaryloxy group, a C₁-C₆₀ heteroarylthio group, a         C₂-C₆₀ heteroarylalkyl group, a monovalent non-aromatic         condensed polycyclic group, and a monovalent non-aromatic         condensed heteropolycyclic group, each substituted with at least         one selected from deuterium, —F, —Cl, —Br, —I, —CD₃, —CD₂H,         —CDH₂, a hydroxyl group, a cyano group, a nitro group, an         amidino group, a hydrazine group, a hydrazone group, a         carboxylic acid group or a salt thereof, a sulfonic acid group         or a salt thereof, a phosphoric acid group or a salt thereof, a         C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl         group, a C₁-C₆₀ alkoxy group, a C₃-C₁₀ cycloalkyl group, a         C₁-C₁₀ heterocycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a         C₁-C₁₀ heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₆-C₆₀         aryloxy group, a C₆-C₆₀ arylthio group, a C₇-C₆₀ arylalkyl         group, a C₁-C₆₀ heteroaryl group, a C₁-C₆₀ heteroaryloxy group,         a C₁-C₆₀ heteroarylthio group, a C₂-C₆₀ heteroarylalkyl group, a         monovalent non-aromatic condensed polycyclic group, a monovalent         non-aromatic condensed heteropolycyclic group, —N(Q₂₁)(Q₂₂),         —Si(Q₂₃)(Q₂₄)(Q₂₅), —B(Q₂₆)(Q₂₇), and —P(═O)(Q₂₈)(Q₂₉); and     -   —N(Q₃₁)(Q₃₂), —Si(Q₃₃)(Q₃₄)(Q₃₅), —B(Q₃₆)(Q₃₇), and         —P(═O)(Q₃₈)(Q₃₉),     -   Q₁ to Q₉, Q₁₁ to Q₁₉, Q₂₁ to Q₂₉, and Q₃₁ to Q₃₉ may each         independently be selected from hydrogen, deuterium, —F, —Cl,         —Br, —I, a hydroxyl group, a cyano group, a nitro group, an         amidino group, a hydrazine group, a hydrazone group, a         carboxylic acid group or a salt thereof, a sulfonic acid group         or a salt thereof, a phosphoric acid group or a salt thereof, a         C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl         group, a C₁-C₆₀ alkoxy group, a C₃-C₁₀ cycloalkyl group, a         C₁-C₁₀ heterocycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a         C₁-C₁₀ heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₆-C₆₀         aryl group substituted with at least one selected from a C₁-C₆₀         alkyl group and a C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a         C₆-C₆₀ arylthio group, a C₇-C₆₀ arylalkyl group, a C₁-C₆₀         heteroaryl group, a C₁-C₆₀ heteroaryloxy group, a C₁-C₆₀         heteroarylthio group, a C₂-C₆₀ heteroarylalkyl group, a         monovalent non-aromatic condensed polycyclic group, and a         monovalent non-aromatic condensed heteropolycyclic group, and     -   Formula 1 satisfies at least one of Condition 1 to Condition 4:     -   Condition 1     -   CY₁ in Formula 1 is a group represented by Formula CZ1, provided         that at least one of X₁₁ to X₁₇ in Formula CZ1 is each         independently N or C(CN),     -   Condition 2     -   at least one of X₂₁ to X₂₆ in Formula 1 is each independently N         or C(CN),     -   Condition 3     -   CY₃ in Formula 1 is a group represented by Formula CZ3, provided         that at least one of X₃₁ to X₃₆ in Formula CZ3 is each         independently N or C(CN), and     -   Condition 4     -   CY₄ in Formula 1 is a group represented by Formula CZ4, provided         that at least one of X₄₁ to X₄₇ in Formula CZ4 is each         independently N or C(CN).

According to one or more embodiments, an organic light-emitting device includes: a first electrode; a second electrode; and an organic layer that is disposed between the first electrode and the second electrode and includes an emission layer and at least one organometallic compound.

The organometallic compound may act as a dopant in the organic layer.

According to one or more embodiments, a diagnostic composition includes at least one organometallic compound represented by Formula 1.

BRIEF DESCRIPTION OF THE DRAWINGS

These and/or other aspects will become apparent and more readily appreciated from the following description of the embodiments, taken in conjunction with the accompanying drawings in which:

FIG. 1 is a schematic view of an organic light-emitting device according to an embodiment; and

FIG. 2 is a graph of photoluminescence (PL) intensity (arbitrary units, a.u.) versus wavelength (nanometers, nm) showing photoluminescence spectra of Compounds 1, 2, A, 7, 24, and B.

DETAILED DESCRIPTION

Reference will now be made in detail to embodiments, examples of which are illustrated in the accompanying drawings, wherein like reference numerals refer to like elements throughout. In this regard, the present embodiments may have different forms and should not be construed as being limited to the descriptions set forth herein. Accordingly, the embodiments are merely described below, by referring to the figures, to explain aspects of the present description. As used herein, the term “and/or” includes any and all combinations of one or more of the associated listed items. Expressions such as “at least one of,” when preceding a list of elements, modify the entire list of elements and do not modify the individual elements of the list.

It will be understood that when an element is referred to as being “on” another element, it can be directly in contact with the other element or intervening elements may be present therebetween. In contrast, when an element is referred to as being “directly on” another element, there are no intervening elements present.

It will be understood that, although the terms first, second, third etc. may be used herein to describe various elements, components, regions, layers, and/or sections, these elements, components, regions, layers, and/or sections should not be limited by these terms. These terms are only used to distinguish one element, component, region, layer, or section from another element, component, region, layer, or section. Thus, a first element, component, region, layer, or section discussed below could be termed a second element, component, region, layer, or section without departing from the teachings of the present embodiments.

The terminology used herein is for the purpose of describing particular embodiments only and is not intended to be limiting. As used herein, the singular forms “a,” “an,” and “the” are intended to include the plural forms as well, unless the context clearly indicates otherwise.

The term “or” means “and/or.” It will be further understood that the terms “comprises” and/or “comprising,” or “includes” and/or “including” when used in this specification, specify the presence of stated features, regions, integers, steps, operations, elements, and/or components, but do not preclude the presence or addition of one or more other features, regions, integers, steps, operations, elements, components, and/or groups thereof.

Unless otherwise defined, all terms (including technical and scientific terms) used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this general inventive concept belongs. It will be further understood that terms, such as those defined in commonly used dictionaries, should be interpreted as having a meaning that is consistent with their meaning in the context of the relevant art and the present disclosure, and will not be interpreted in an idealized or overly formal sense unless expressly so defined herein.

Exemplary embodiments are described herein with reference to cross section illustrations that are schematic illustrations of idealized embodiments. As such, variations from the shapes of the illustrations as a result, for example, of manufacturing techniques and/or tolerances, are to be expected. Thus, embodiments described herein should not be construed as limited to the particular shapes of regions as illustrated herein but are to include deviations in shapes that result, for example, from manufacturing. For example, a region illustrated or described as flat may, typically, have rough and/or nonlinear features. Moreover, sharp angles that are illustrated may be rounded. Thus, the regions illustrated in the figures are schematic in nature and their shapes are not intended to illustrate the precise shape of a region and are not intended to limit the scope of the present claims.

“About” or “approximately” as used herein is inclusive of the stated value and means within an acceptable range of deviation for the particular value as determined by one of ordinary skill in the art, considering the measurement in question and the error associated with measurement of the particular quantity (i.e., the limitations of the measurement system). For example, “about” can mean within one or more standard deviations, or within ±30%, 20%, 10%, 5% of the stated value.

In an embodiment, an organometallic compound is provided. The organometallic compound according to an embodiment may be represented by Formula 1:

M in Formula 1 may be selected from a first-row transition metal of the Periodic Table of Elements, a second-row transition metal of the Periodic Table of Elements, and a third-row transition metal of the Periodic Table of Elements.

For example, M in Formula 1 may be platinum (Pt) or palladium (Pd), but embodiments of the present disclosure are not limited thereto.

The organometallic compound represented by Formula 1 may be a neutral compound that does not consist of an ion pair of an anion and a cation.

X₁ to X₄ in Formula 1 may each independently be C or N.

In Formula 1, two bonds selected from a bond between X₁ and M, a bond between X₂ and M, a bond between X₃ and M, and a bond between X₄ and M may each be a coordinate bond, and the others thereof may each be a covalent bond.

In one or more embodiments, in Formula 1,

-   -   i) X₁ and X₄ may each be N, X₂ and X₃ may each be C, a bond         between X₁ and M and a bond between X₄ and M may each be a         coordinate bond, and a bond between X₂ and M and a bond between         X₃ and M may each be a covalent bond;     -   ii) X₁ and X₃ may each be N, X₂ and X₄ may each be C, a bond         between X₁ and M and a bond between X₃ and M may each be a         coordinate bond, and a bond between X₂ and M and a bond between         X₄ and M may each be a covalent bond; or     -   iii) X₃ and X₄ may each be N, X₁ and X₂ may each be C, a bond         between X₃ and M and a bond between X₄ and M may each be a         coordinate bond, and a bond between X₁ and M and a bond between         X₂ and M may each be a covalent bond.

In Formula 1, Y₂ to Y₅ may each independently be C or N, and Y₁ and Y₆ may each independently be C, N, O, Si, or S.

In Formula 1, a bond between X₁ and Y₁, a bond between X₁ and Y₂, a bond between X₃ and Y₃, a bond between X₃ and Y₄, a bond between X₄ and Y₅, and a bond between X₄ and Y₆ may each be a chemical bond that links the corresponding atoms.

In Formula 1, CY₁ may be selected from a C₅-C₃₀ carbocyclic group, a C₁-C₃₀ heterocyclic group, and a group represented by Formula CZ1, CY₃ may be selected from a C₅-C₃₀ carbocyclic group, a C₁-C₃₀ heterocyclic group, and a group represented by Formula CZ3, and CY₄ may be selected from a C₅-C₃₀ carbocyclic group, a C₁-C₃₀ heterocyclic group, and a group represented by Formula CZ4:

Formulae CZ1, CZ3, and CZ4 are each independently the same as described below.

In an embodiment, in Formula 1, CY₁, CY₃, and CY₄ may each independently be selected from a benzene group, a naphthalene group, an anthracene group, a phenanthrene group, a triphenylene group, a pyrene group, a chrysene group, a cyclopentadiene group, a 1,2,3,4-tetrahydronaphthalene group, a pyrrole group, a thiophene group, a furan group, an indole group, an iso-indole group, a benzoborole group, a benzophosphole group, an indene group, a benzosilole group, a benzogermole group, a benzothiophene group, a benzoselenophene group, a benzofuran group, a carbazole group, a dibenzoborole group, a dibenzophosphole group, a fluorene group, a dibenzosilole group, a dibenzogermole group, a dibenzothiophene group, a dibenzoselenophene group, a dibenzofuran group, a dibenzothiophene 5-oxide group, a 9H-fluorene-9-on group, a dibenzothiophene 5,5-dioxide group, an azacarbazole group, an azadibenzoborole group, an azadibenzophosphole group, an azafluorene group, an azadibenzosilole group, an azadibenzogermole group, an azadibenzothiophene group, an azadibenzoselenophene group, an azadibenzofuran group, an azadibenzothiophene 5-oxide group, an aza-9H-fluorene-9-on group, an azadibenzothiophene 5,5-dioxide group, a pyridine group, a pyrimidine group, a pyrazine group, a pyridazine group, a triazine group, a quinoline group, an isoquinoline group, a quinoxaline group, a quinazoline group, a phenanthroline group, a pyrazole group, an imidazole group, a triazole group, a tetrazole group, an oxazole group, an isoxazole group, a thiazole group, an isothiazole group, an oxadiazole group, a thiadiazole group, a benzopyrazole group, a benzimidazole group, a benzoxazole group, a benzothiazole group, a benzoxadiazole group, a benzothiadiazole group, a 5,6,7,8-tetrahydroisoquinoline group, and a 5,6,7,8-tetrahydroquinoline group; CY₁ may be a group represented by Formula CZ1; CY₃ may be a group represented by Formula CZ3; or CY₄ may be a group represented by Formula CZ4.

For example, in Formula 1, CY₁, CY₃, and CY₄ may each independently be selected from a benzene group, a naphthalene group, a pyrrole group, a thiophene group, a furan group, an indole group, an iso-indole group, a pyridine group, a pyrimidine group, a pyrazine group, a pyridazine group, a quinoline group, an isoquinoline group, a pyrazole group, an imidazole group, a triazole group, a tetrazole group, an oxazole group, an isoxazole group, a thiazole group, an isothiazole group, an oxadiazole group, a thiadiazole group, a benzopyrazole group, a benzimidazole group, a benzoxazole group, a benzothiazole group, a benzoxadiazole group, a benzothiadiazole group, a 5,6,7,8-tetrahydroisoquinoline group, and a 5,6,7,8-tetrahydroquinoline group; CY₁ may be a group represented by Formula CZ1; CY₃ may be a group represented by Formula CZ3; or CY₄ may be a group represented by Formula CZ4, but embodiments of the present disclosure are not limited thereto.

“An azacarbazole group, an azadibenzoborole group, an azadibenzophosphole group, an azafluorene group, an azadibenzosilole group, an azadibenzogermole group, an azadibenzothiophene group, an azadibenzoselenophene group, an azadibenzofuran group, an azadibenzothiophene 5-oxide group, an aza-9H-fluorene-9-on group, and an azadibenzothiophene 5,5-dioxide group” as used herein mean hetero-rings that respectively have the same backbones as “a carbazole group, a dibenzoborole group, a dibenzophosphole group, a fluorene group, a dibenzosilole group, a dibenzogermole group, a dibenzothiophene group, a dibenzoselenophene group, a dibenzofuran group, a dibenzothiophene 5-oxide group, a 9H-fluorene-9-on group, and a dibenzothiophene 5,5-dioxide group”, provided that at least one of carbons forming rings thereof is substituted with nitrogen.

In one or more embodiments, CY₁ and CY₄ in Formula 1 may be identical to each other.

In one or more embodiments, in Formula 1,

a moiety represented by

and a moiety represented by

may be identical to each other;

a moiety represented by

and a moiety represented by

may be identical to each other;

a moiety represented by

and a moiety represented by

may be identical to each other;

a moiety represented by

may be identical to each other; or

a moiety represented by

a moiety represented by

a moiety represented by

and a moiety represented by

may be different from one another.

In one or more embodiments, the organometallic compound may have a symmetrical structure with respect to an axis connecting M and T₂ in Formula 1.

T₁ to T₃ in Formula 1 may each independently be selected from *—N[(L₅)_(b5)-(R₅)]—*′, *—B(R₅)—*′, *—P(R₅)—*′, *—C(R₅)(R₆)—*′, *—Si(R₅)(R₆)—*′, *—Ge(R₅)(R₆)—*′, *—S—*′, *—Se—*′, *—O—*′, *—C(═O)—*′, *—S(═O)—*′, *—S(═O)₂—*′, *—C(R₅)═*′, *═C(R₅)—*′, *—C(R₅)═C(R₆)—*′, *—C(═S)—*′, and *—C≡C—*′. R₅ and R₆ are each independently the same as described below.

L₅ may be selected from a single bond, a substituted or unsubstituted C₅-C₃₀ carbocyclic group, and a substituted or unsubstituted C₁-C₃₀ heterocyclic group, and b5 may be selected from 1 to 3 (for example, b5 may be 1), wherein, when b5 is two or more, two or more groups L₅ may be identical to or different from each other.

In an embodiment, L₅ may be selected from:

-   -   a single bond, a phenylene group, a naphthylene group, a         fluorenylene group, a pyridinylene group, a pyrimidinylene         group, and a carbazolylene group; and     -   a phenylene group, a naphthylene group, a fluorenylene group, a         pyridinylene group, a pyrimidinylene group, and a carbazolylene         group, each substituted with at least one selected from         deuterium, —F, —Cl, —Br, —I, —CD₃, —CD₂H, —CDH₂, —CF₃, —CF₂H,         —CFH₂, a hydroxyl group, a cyano group, a nitro group, an amino         group, an amidino group, a hydrazine group, a hydrazone group, a         carboxylic acid group or a salt thereof, a sulfonic acid group         or a salt thereof, a phosphoric acid group or a salt thereof, a         C₁-C₂₀ alkyl group, a C₁-C₂₀ alkoxy group, a phenyl group, a         naphthyl group, a biphenyl group, and a terphenyl group,     -   but embodiments of the present disclosure are not limited         thereto.

R₅ and R₆ may optionally be linked via a first linking group to form a substituted or unsubstituted C₅-C₃₀ carbocyclic group or a substituted or unsubstituted C₁-C₃₀ heterocyclic group (for example, a C₅-C₆ 5-membered to 7-membered cyclic group; or a C₅-C₆ 5-membered to 7-membered cyclic group substituted with at least one deuterium, a cyano group, —F, a C₁-C₁₀ alkyl group, and a C₆-C₁₄ aryl group).

In an embodiment, T₁ to T₃ in Formula 1 may each independently be selected from *—N[(L₅)_(b5)-(R₅)]—*′, *—B(R₅)—*′, *—C(R₅)(R₆)—*′, *—Si(R₅)(R₆)—*′, *—S—*′, or *—O—*′, but embodiments of the present disclosure are not limited thereto.

In one or more embodiments, T₁ to T₃ in Formula 1 may each independently be selected from *—C(R₅)(R₆)—*′, *—Si(R₅)(R₆)—*′, and *—Ge(R₅)(R₆)—*′,

-   -   R₅ and R₆ may be linked via a first linking group.

The first linking group may be selected from a single bond, *—N[(L₉)_(b9)-(R₉)]—*′, *—B(R₉)—*′, *—P(R₉)—*′, *—C(R₉)(R₁₀)—*′, *—Si(R₉)(R₁₀)—*′, *—Ge(R₉)(R₁₀)—*′, *—S—*′, *—Se—*′, *—O—*′, *—C(═O)—*′, *—S(═O)—*′, *—S(═O)₂—*′, *—C(R₉)═C(R₁₀)—*′, *—C(═S)—*″, and *—C≡C—*′,

-   -   L₉ and b9 are each independently the same as described in         connection with L₅ and b5,     -   R₉ and R₁₀ are each independently the same as described in         connection with R₅, and     -   * and *′ each indicate a binding site to a neighboring atom, but         embodiments of the present disclosure are not limited thereto.

n1, n2, and n3 in Formula 1 respectively indicate the number of groups T₁, the number of groups T₂, and the number of groups T₃, and may each independently be 0, 1, 2, or 3, wherein, when n1 is zero, *-(T₁)_(n1)-*′ may be a single bond, when n2 is zero, *-(T₂)_(n2)-*′ may be a single bond, and when n3 is zero, *-(T₃)_(n3)-*′ may be a single bond. When n1 is two or more, two or more groups T₁ may be identical to or different from each other, when n2 is two or more, two or more groups T₂ may be identical to or different from each other, and when n3 is two or more, two or more groups T₃ may be identical to or different from each other.

In an embodiment, n1 to n3 in Formula 1 may each independently 0 or 1.

In one or more embodiments, the sum of n1, n2, and n3 may be 1 or 2.

In one or more embodiments, in Formula 1, i) n1 and n3 may each be 0 and n2 may be 1; or ii) n1 may be 0 and n2 and n3 may each be 1, but embodiments of the present disclosure are not limited thereto.

In Formulae CZ1, CZ3, and CZ4, X₁₁ may be N or C(R₁₁), X₁₂ may be N or C(R₁₂), X₁₃ may be N or C(R₁₃), X₁₄ may be N or C(R₁₄), X₁₅ may be N or C(R₁₅), X₁₆ may be N or C(R₁₆), X₁₇ may be N or C(R₁₇), X₂₁ may be N or C(R₂₁), X₂₂ may be N or C(R₂₂), X₂₃ may be N or C(R₂₃), X₂₄ may be N or C(R₂₄), X₂₅ may be N or C(R₂₅), X₂₆ may be N or C(R₂₆), X₃₁ may be N or C(R₃₁), X₃₂ may be N or C(R₃₂), X₃₃ may be N or C(R₃₃), X₃₄ may be N or C(R₃₄), X₃₅ may be N or C(R₃₅), X₃₆ may be N or C(R₃₆), X₄₁ may be N or C(R₄₁), X₄₂ may be N or C(R₄₂), X₄₃ may be N or C(R₄₃), X₄₄ may be N or C(R₄₄), X₄₅ may be N or C(R₄₅), X₄₆ may be N or C(R₄₆), and X₄₇ may be N or C(R₄₇).

Formula 1 may satisfy at least one of Condition 1 to Condition 4:

-   -   Condition 1     -   CY₁ in Formula 1 is a group represented by Formula CZ1, provided         that at least one of X₁₁ to X₁₇ in Formula CZ1 is each         independently N or C(CN),     -   Condition 2     -   at least one of X₂₁ to X₂₆ in Formula 1 is each independently N         or C(CN),     -   Condition 3     -   CY₃ in Formula 1 is a group represented by Formula CZ3, provided         that at least one of X₃₁ to X₃₆ in Formula CZ3 is each         independently N or C(CN), and     -   Condition 4     -   CY₄ in Formula 1 is a group represented by Formula CZ4, provided         that at least one of X₄₁ to X₄₇ in Formula CZ4 is each         independently N or C(CN).

For example, in Formula 1,

-   -   i) when CY₁ is not a group represented by Formula CZ1, CY₃ is         not a group represented by Formula CZ3, and CY₄ is not a group         represented by Formula CZ4, at least one of X₂₁ to X₂₆ (for         example, one or two of X₂₁ to X₂₆) may each independently be N         or C(CN),     -   ii) when CY₁ is a group represented by Formula CZ1, at least one         of X₁₁ to X₁₇ and X₂₁ to X₂₆ (for example, one or two of X₁₁ to         X₁₇ and X₂₁ to X₂₆) may each independently be N or C(CN),     -   iii) when CY₃ is a group represented by Formula CZ3, at least         one of X₂₁ to X₂₆ and X₃₁ to X₃₆ (for example, one or two of X₂₁         to X₂₆ and X₃₁ to X₃₆) may each independently be N or C(CN), and     -   iv) when CY₄ is a group represented by Formula CZ4, at least one         of X₂₁ to X₂₆ and X₄₁ to X₄₇ (for example, one or two of X₂₁ to         X₂₆ and X₄₁ to X₄₇) may each independently be N or C(CN).

R₁, R₃ to R₆, R₁₁ to R₁₇, R₂₁ to R₂₆, R₃₁ to R₃₆, and R₄₁ to R₄₇ may each independently be selected from hydrogen, deuterium, —F, —Cl, —Br, —I, —SF₅, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a substituted or unsubstituted C₁-C₆₀ alkyl group, a substituted or unsubstituted C₂-C₆₀ alkenyl group, a substituted or unsubstituted C₂-C₆₀ alkynyl group, a substituted or unsubstituted C₁-C₆₀ alkoxy group, a substituted or unsubstituted C₃-C₁₀ cycloalkyl group, a substituted or unsubstituted C₁-C₁₀ heterocycloalkyl group, a substituted or unsubstituted C₃-C₁₀ cycloalkenyl group, a substituted or unsubstituted C₁-C₁₀ heterocycloalkenyl group, a substituted or unsubstituted C₆-C₆₀ aryl group, a substituted or unsubstituted C₆-C₆₀ aryloxy group, a substituted or unsubstituted C₆-C₆₀ arylthio group, a substituted or unsubstituted C₇-C₆₀ arylalkyl group, a substituted or unsubstituted C₁-C₆₀ heteroaryl group, a substituted or unsubstituted C₁-C₆₀ heteroaryloxy group, a substituted or unsubstituted C₁-C₆₀ heteroarylthio group, a substituted or unsubstituted C₂-C₆₀ heteroarylalkyl group, a substituted or unsubstituted monovalent non-aromatic condensed polycyclic group, a substituted or unsubstituted monovalent non-aromatic condensed heteropolycyclic group, —N(Q₁)(Q₂), —Si(Q₃)(Q₄)(Q₅), —B(Q₆)(Q₇), and —P(═O)(Q₈)(Q₉). Q₁ to Q₉ are each independently the same as described herein.

For example, R₁, R₃ to R₆, R₁₁ to R₁₇, R₂₁ to R₂₆, R₃₁ to R₃₆, and R₄₁ to R₄₇ may each independently be selected from:

-   -   hydrogen, deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano         group, a nitro group, an amino group, an amidino group, a         hydrazine group, a hydrazone group, a carboxylic acid group or a         salt thereof, a sulfonic acid group or a salt thereof, a         phosphoric acid group or a salt thereof, —SF₅, C₁-C₂₀ alkyl         group, and a C₁-C₂₀ alkoxy group;     -   a C₁-C₂₀ alkyl group and a C₁-C₂₀ alkoxy group, each substituted         with at least one selected from deuterium, —F, —Cl, —Br, —I,         —CD₃, —CD₂H, —CDH₂, —CF₃, —CF₂H, —CFH₂, a hydroxyl group, a         cyano group, a nitro group, an amino group, an amidino group, a         hydrazine group, a hydrazone group, a carboxylic acid group or a         salt thereof, a sulfonic acid group or a salt thereof, a         phosphoric acid group or a salt thereof, a C₁-C₁₀ alkyl group, a         cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a         cyclooctyl group, an adamantanyl group, a norbornanyl group, a         norbornenyl group, a cyclopentenyl group, a cyclohexenyl group,         a cycloheptenyl group, a phenyl group, a naphthyl group, a         pyridinyl group, and a pyrimidinyl group;     -   a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a         cyclooctyl group, an adamantanyl group, a norbornanyl group, a         norbornenyl group, a cyclopentenyl group, a cyclohexenyl group,         a cycloheptenyl group, a phenyl group, a naphthyl group, a         fluorenyl group, a phenanthrenyl group, an anthracenyl group, a         fluoranthenyl group, a triphenylenyl group, a pyrenyl group, a         chrysenyl group, a pyrrolyl group, a thiophenyl group, a furanyl         group, an imidazolyl group, a pyrazolyl group, a thiazolyl         group, an isothiazolyl group, an oxazolyl group, an isoxazolyl         group, a pyridinyl group, a pyrazinyl group, a pyrimidinyl         group, a pyridazinyl group, an isoindolyl group, an indolyl         group, an indazolyl group, a purinyl group, a quinolinyl group,         an isoquinolinyl group, a benzoquinolinyl group, a quinoxalinyl         group, a quinazolinyl group, a cinnolinyl group, a carbazolyl         group, a phenanthrolinyl group, a benzimidazolyl group, a         benzofuranyl group, a benzothiophenyl group, an         isobenzothiazolyl group, a benzoxazolyl group, an         isobenzoxazolyl group, a triazolyl group, a tetrazolyl group, an         oxadiazolyl group, a triazinyl group, a dibenzofuranyl group, a         dibenzothiophenyl group, a benzocarbazolyl group, a         dibenzocarbazolyl group, an imidazopyridinyl group, and an         imidazopyrimidinyl group;     -   a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a         cyclooctyl group, an adamantanyl group, a norbornanyl group, a         norbornenyl group, a cyclopentenyl group, a cyclohexenyl group,         a cycloheptenyl group, a phenyl group, a naphthyl group, a         fluorenyl group, a phenanthrenyl group, an anthracenyl group, a         fluoranthenyl group, a triphenylenyl group, a pyrenyl group, a         chrysenyl group, a pyrrolyl group, a thiophenyl group, a furanyl         group, an imidazolyl group, a pyrazolyl group, a thiazolyl         group, an isothiazolyl group, an oxazolyl group, an isoxazolyl         group, a pyridinyl group, a pyrazinyl group, a pyrimidinyl         group, a pyridazinyl group, an isoindolyl group, an indolyl         group, an indazolyl group, a purinyl group, a quinolinyl group,         an isoquinolinyl group, a benzoquinolinyl group, a quinoxalinyl         group, a quinazolinyl group, a cinnolinyl group, a carbazolyl         group, a phenanthrolinyl group, a benzimidazolyl group, a         benzofuranyl group, a benzothiophenyl group, an         isobenzothiazolyl group, a benzoxazolyl group, an         isobenzoxazolyl group, a triazolyl group, a tetrazolyl group, an         oxadiazolyl group, a triazinyl group, a dibenzofuranyl group, a         dibenzothiophenyl group, a benzocarbazolyl group, a         dibenzocarbazolyl group, an imidazopyridinyl group, and an         imidazopyrimidinyl group, each substituted with at least one         selected from deuterium, —F, —Cl, —Br, —I, —CD₃, —CD₂H, —CDH₂,         —CF₃, —CF₂H, —CFH₂, a hydroxyl group, a cyano group, a nitro         group, an amino group, an amidino group, a hydrazine group, a         hydrazone group, a carboxylic acid group or a salt thereof, a         sulfonic acid group or a salt thereof, a phosphoric acid group         or a salt thereof, a C₁-C₂₀ alkyl group, a C₁-C₂₀ alkoxy group,         a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a         cyclooctyl group, an adamantanyl group, a norbornanyl group, a         norbornenyl group, a cyclopentenyl group, a cyclohexenyl group,         a cycloheptenyl group, a phenyl group, a naphthyl group, a         fluorenyl group, a phenanthrenyl group, an anthracenyl group, a         fluoranthenyl group, a triphenylenyl group, a pyrenyl group, a         chrysenyl group, a pyrrolyl group, a thiophenyl group, a furanyl         group, an imidazolyl group, a pyrazolyl group, a thiazolyl         group, an isothiazolyl group, an oxazolyl group, an isoxazolyl         group, a pyridinyl group, a pyrazinyl group, a pyrimidinyl         group, a pyridazinyl group, an isoindolyl group, an indolyl         group, an indazolyl group, a purinyl group, a quinolinyl group,         an isoquinolinyl group, a benzoquinolinyl group, a quinoxalinyl         group, a quinazolinyl group, a cinnolinyl group, a carbazolyl         group, a phenanthrolinyl group, a benzimidazolyl group, a         benzofuranyl group, a benzothiophenyl group, an         isobenzothiazolyl group, a benzoxazolyl group, an         isobenzoxazolyl group, a triazolyl group, a tetrazolyl group, an         oxadiazolyl group, a triazinyl group, a dibenzofuranyl group, a         dibenzothiophenyl group, a benzocarbazolyl group, a         dibenzocarbazolyl group, an imidazopyridinyl group, and an         imidazopyrimidinyl group; and     -   —N(Q₁)(Q₂), —Si(Q₃)(Q₄)(Q₅), —B(Q₆)(Q₇), and —P(═O)(Q₈)(Q₉), and     -   Q₁ to Q₉ may each independently be selected from:     -   —CH₃, —CD₃, —CD₂H, —CDH₂, —CH₂CH₃, —CH₂CD₃, —CH₂CD₂H, —CH₂CDH₂,         —CHDCH₃, —CHDCD₂H, —CHDCDH₂, —CHDCD₃, —CD₂CD₃, —CD₂CD₂H, and         —CD₂CDH₂;     -   an n-propyl group, an iso-propyl group, an n-butyl group, an         iso-butyl group, a sec-butyl group, a tert-butyl group, an         n-pentyl group, an iso-pentyl group, a sec-pentyl group, a         tert-pentyl group, a phenyl group, and a naphthyl group; and     -   an n-propyl group, an iso-propyl group, an n-butyl group, an         iso-butyl group, a sec-butyl group, a tert-butyl group, an         n-pentyl group, an iso-pentyl group, a sec-pentyl group, a         tert-pentyl group, a phenyl group, and a naphthyl group, each         substituted with at least one selected from deuterium, a C₁-C₁₀         alkyl group, and a phenyl group.

In an embodiment, R₁, R₃ to R₆, R₁₁ to R₁₇, R₂₁ to R₂₆, R₃₁ to R₃₆, and R₄₁ to R₄₇ may each independently be selected from:

-   -   hydrogen, deuterium, —F, a cyano group, a nitro group, —SF₅, a         methyl group, an ethyl group, an n-propyl group, an iso-propyl         group, an n-butyl group, an iso-butyl group, a sec-butyl group,         a tert-butyl group, an n-pentyl group, an iso-pentyl group, a         sec-pentyl group, a tert-pentyl group, an n-hexyl group, an         iso-hexyl group, a sec-hexyl group, a tert-hexyl group, an         n-heptyl group, an iso-heptyl group, a sec-heptyl group, a         tert-heptyl group, an n-octyl group, an iso-octyl group, a         sec-octyl group, a tert-octyl group, an n-nonyl group, an         iso-nonyl group, a sec-nonyl group, a tert-nonyl group, an         n-decyl group, an iso-decyl group, a sec-decyl group, a         tert-decyl group, a methoxy group, an ethoxy group, a propoxy         group, a butoxy group, a pentoxy group, a cyclopentyl group, a         cyclohexyl group, a cycloheptyl group, a cyclooctyl group, an         adamantanyl group, a norbornanyl group, a norbornenyl group, a         cyclopentenyl group, a cyclohexenyl group, a cycloheptenyl         group, a phenyl group, a naphthyl group, a pyridinyl group, a         pyrimidinyl group, a carbazolyl group, a dibenzofuranyl group,         and a dibenzothiophenyl group;     -   a methyl group, an ethyl group, an n-propyl group, an iso-propyl         group, an n-butyl group, an iso-butyl group, a sec-butyl group,         a tert-butyl group, an n-pentyl group, an iso-pentyl group, a         sec-pentyl group, a tert-pentyl group, an n-hexyl group, an         iso-hexyl group, a sec-hexyl group, a tert-hexyl group, an         n-heptyl group, an iso-heptyl group, a sec-heptyl group, a         tert-heptyl group, an n-octyl group, an iso-octyl group, a         sec-octyl group, a tert-octyl group, an n-nonyl group, an         iso-nonyl group, a sec-nonyl group, a tert-nonyl group, an         n-decyl group, an iso-decyl group, a sec-decyl group, a         tert-decyl group, a methoxy group, an ethoxy group, a propoxy         group, a butoxy group, a pentoxy group, a cyclopentyl group, a         cyclohexyl group, a cycloheptyl group, a cyclooctyl group, an         adamantanyl group, a norbornanyl group, a norbornenyl group, a         cyclopentenyl group, a cyclohexenyl group, a cycloheptenyl         group, a phenyl group, a naphthyl group, a pyridinyl group, a         pyrimidinyl group, a carbazolyl group, a dibenzofuranyl group,         and a dibenzothiophenyl group, each substituted with at least         one selected from deuterium, —F, —CD₃, —CD₂H, —CDH₂, —CF₃,         —CF₂H, —CFH₂, a cyano group, a nitro group, a C₁-C₁₀ alkyl         group, a C₁-C₁₀ alkoxy group, a cyclopentyl group, a cyclohexyl         group, a cycloheptyl group, a cyclooctyl group, an adamantanyl         group, a norbornanyl group, a norbornenyl group, a cyclopentenyl         group, a cyclohexenyl group, a cycloheptenyl group, a phenyl         group, a naphthyl group, a pyridinyl group, a pyrimidinyl group,         a carbazolyl group, a dibenzofuranyl group, and a         dibenzothiophenyl group; and     -   —N(Q₁)(Q₂), —Si(Q₃)(Q₄)(Q₅), —B(Q₆)(Q₇), and —P(═O)(Q₈)(Q₉), and     -   Q₁ to Q₉ are each independently the same as described above.

In one or more embodiments, R₁, R₃ to R₆, R₁₁ to R₁₇, R₂₁ to R₂₆, R₃₁ to R₃₆, and R₄₁ to R₄₇ may each independently be selected from hydrogen, deuterium, —F, a cyano group, a nitro group, —SF₅, —CH₃, —CD₃, —CD₂H, —CDH₂, —CF₃, —CF₂H, —CFH₂, groups represented by Formulae 9-1 to 9-19, groups represented by Formulae 10-1 to 10-139, and —Si(Q₃)(Q₄)(Q₅) (wherein Q₃ to Q₅ are each independently the same as described herein), but embodiments of the present disclosure are not limited thereto:

In Formulae 9-1 to 9-19 and 10-1 to 10-139, “Ph” indicates a phenyl group, “TMS” indicates a trimethylsilyl group, and * indicates a binding site to a neighboring atom.

a1, a3, and a4 in Formula 1 respectively indicate the number of groups R₁, the number of groups R₃, and the number of groups R₄, and may each independently be 0, 1, 2, 3, 4, or 5. When a1 is two or more, two or more groups R₁ may be identical to or different from each other, when a3 is two or more, two or more groups R₃ may be identical to or different from each other, and when a4 is two or more, two or more groups R₄ may be identical to or different from each other, but embodiments of the present disclosure are not limited thereto.

In Formula 1, two of groups R₁ in the number of a1 may optionally be linked to form a substituted or unsubstituted C₅-C₃₀ carbocyclic group or a substituted or unsubstituted C₁-C₃₀ heterocyclic group, two of groups R₃ in the number of a3 may optionally be linked to form a substituted or unsubstituted C₅-C₃₀ carbocyclic group or a substituted or unsubstituted C₁-C₃₀ heterocyclic group, two of groups R₄ in the number of a4 may optionally be linked to form a substituted or unsubstituted C₅-C₃₀ carbocyclic group or a substituted or unsubstituted C₁-C₃₀ heterocyclic group, two of R₁₁ to R₁₇ may optionally be linked to form a substituted or unsubstituted C₅-C₃₀ carbocyclic group or a substituted or unsubstituted C₁-C₃₀ heterocyclic group, two of R₂₁ to R₂₆ may optionally be linked to form a substituted or unsubstituted C₅-C₃₀ carbocyclic group or a substituted or unsubstituted C₁-C₃₀ heterocyclic group, two of R₃₁ to R₃₆ may optionally be linked to form a substituted or unsubstituted C₅-C₃₀ carbocyclic group or a substituted or unsubstituted C₁-C₃₀ heterocyclic group, and two of R₄₁ to R₄₇ may optionally be linked to form a substituted or unsubstituted C₅-C₃₀ carbocyclic group or a substituted or unsubstituted C₁-C₃₀ heterocyclic group.

For example, i) a substituted or unsubstituted C₅-C₃₀ carbocyclic group or a substituted or unsubstituted C₁-C₃₀ heterocyclic group, formed by linking two of groups R₁ in the number of a1, ii) a substituted or unsubstituted C₅-C₃₀ carbocyclic group or a substituted or unsubstituted C₁-C₃₀ heterocyclic group, formed by linking two of groups R₃ in the number of a3, iii) a substituted or unsubstituted C₅-C₃₀ carbocyclic group or a substituted or unsubstituted C₁-C₃₀ heterocyclic group, two of groups R₄ in the number of a4, iv) a substituted or unsubstituted C₅-C₃₀ carbocyclic group or a substituted or unsubstituted C₁-C₃₀ heterocyclic group, formed by linking two of R₁₁ to R₁₇, V) a substituted or unsubstituted C₅-C₃₀ carbocyclic group or a substituted or unsubstituted C₁-C₃₀ heterocyclic group, formed by linking two of R₂₁ to R₂₆, vi) a substituted or unsubstituted C₅-C₃₀ carbocyclic group or a substituted or unsubstituted C₁-C₃₀ heterocyclic group, formed by linking two of R₃₁ to R₃₆, and v) a substituted or unsubstituted C₅-C₃₀ carbocyclic group or a substituted or unsubstituted C₁-C₃₀ heterocyclic group, formed by linking two of R₄₁ to R₄₇, in Formula 1, may each independently be selected from:

-   -   a pentadiene group, a cyclohexane group, a cycloheptane group,         an adamantane group, a bicycle-heptane group, a bicyclo-octane         group, a benzene group, a pyridine group, a pyrimidine group, a         pyrazine group, a pyridazine group, a naphthalene group, an         anthracene group, a tetracene group, a phenanthrene group, a         dihydronaphthalene group, a phenalene group, a benzothiophene         group, a benzofuran group, an indene group, an indole group, a         benzosilole group, an azabenzothiophene group, an azabenzofuran         group, an azaindene group, an azaindole group, and an         azabenzosilole group; and     -   a pentadiene group, a cyclohexane group, a cycloheptane group,         an adamantane group, a bicycle-heptane group, a bicyclo-octane         group, a benzene group, a pyridine group, a pyrimidine group, a         pyrazine group, a pyridazine group, a naphthalene group, an         anthracene group, a tetracene group, a phenanthrene group, a         dihydronaphthalene group, a phenalene group, a benzothiophene         group, a benzofuran group, an indene group, an indole group, a         benzosilole group, an azabenzothiophene group, an azabenzofuran         group, an azaindene group, an azaindole group, and an         azabenzosilole group, each substituted with at least one R₁₀₀,     -   but embodiments of the present disclosure are not limited         thereto.

R₁₀₀ is the same as described in connection with R₁.

In an embodiment, a moiety represented by

in Formula 1 may be selected from groups represented by Formulae CY1-1 to CY1-39 and CZ1-1 to CZ1-8:

In Formula CY1-1 to CY1-39 and CZ1-7 Formula CZ1-8

-   -   X₁ and R₁ are each independently the same as described herein,     -   X₁₈ may be N or C(R₁₈),     -   X₁₉ may be O, S, N[(L₁₉)_(b19)-(R₁₉)], or C(R_(19a))(R_(19b)),     -   R₁₁ to R₁₈ are each independently the same as described in         connection with R₁,     -   L₁₉ and b19 are each independently the same as described in         connection with L₅ and b5,     -   R₁₉, R_(19a), and R_(19b) are each independently the same as         described in connection with R₅,     -   X₁₁ to X₁₇ may each independently be N or C(CN),     -   a15 may be an integer from 0 to 5,     -   a14 may be an integer from 0 to 4,     -   a13 may be an integer from 0 to 3,     -   a12 may be an integer from 0 to 2, and     -   * and *′ each indicate a binding site to a neighboring atom.

In one or more embodiments, a moiety represented by

in Formula 1 may be selected from groups represented by Formulae CZ2-1 to CZ2-7:

In Formulae CZ2-1 to CZ2-7,

-   -   X₂ and R₂₁ to R₂₆ are each independently the same as described         herein,     -   X₂₁ to X₂₆ may each independently be N or C(CN), and     -   *, *′, and *″ each indicate a binding site to a neighboring         atom.

In one or more embodiments, a moiety represented by

in Formula 1 may be selected from groups represented by Formulae CY3-1 to CY3-27 and CZ3-1 to CZ3-7:

In Formulae CY3-1 to CY3-27 and CZ3-1 to CZ3-7,

-   -   X₃ and R₃ are each independently the same as described herein,     -   X₃₈ may be N or C(R₃₈),     -   X₃₉ may be O, S, N[(L₃₉)_(b39)-(R₃₉)], or C(R_(39a))(R_(39b)),     -   R₃₁ to R₃₈ are each independently the same as described in         connection with R₁,     -   L₃₉ and b39 are each independently the same as described in         connection with L₅ and b5,     -   R₃₉, R_(39a), and R_(39b) are each independently the same as         described in connection with R₅,     -   X₃₁ to X₃₆ may each be N or C(CN),     -   a34 may be an integer from 0 to 4,     -   a33 may be an integer from 0 to 3,     -   a32 may be an integer from 0 to 2, and     -   *, *′, and *″ each indicate a binding site to a neighboring         atom.

In one or more embodiments, a moiety represented by

in Formula 1 may be selected from groups represented by Formulae CY4-1 to CY3-39 and CZ4-1 to CZ4-8:

In Formulae CY4-1 to CY4-39 and CZ4-1 to CZ4-8,

-   -   X₄ and R₄ are each independently the same as described herein,     -   X₄₈ may be N or C(R₄₈),     -   X₄₉ may be O, S, N[(L₄₉)_(b49)-(R₄₉)], or C(R_(49a))(R_(49b)),     -   R₄₁ to R₄₈ are each independently the same as described in         connection with R₁,     -   L₄₉ and b49 are each independently the same as described in         connection with L₅ and b5,     -   R₄₉, R_(49a), and R_(49b) are each independently the same as         described in connection with R₅,     -   X₄₁ to X₄₇ may each be N or C(CN),     -   a45 may be an integer from 0 to 5,     -   a44 may be an integer from 0 to 4,     -   a43 may be an integer from 0 to 3,     -   a42 may be an integer from 0 to 2, and     -   * and *′ each indicate a binding site to a neighboring atom.

In one or more embodiments, a moiety represented by

in Formula 1 may be selected from groups represented by Formulae CY1(1) to CY1(8) and CZ1-1 to CZ1-8, and/or

a moiety represented by

in Formula 1 may be selected from groups represented by Formulae CZ2-1 to CZ2-7, and/or

a moiety represented by

in Formula 1 may be selected from groups represented by Formulae CY3(1) to CY3(6) and CZ3-1 to CZ3-7, and/or

a moiety represented by

in Formula 1 may be selected from groups represented by Formulae CY4(1) to CY4(8) and CZ4-1 to CZ4-8:

In Formulae CY1(1) to CY4(9), CY3(1) to CY3(6), and CY4(1) to CY4(9),

-   -   X₁, R₁, X₂, R₂, X₃, R₃, X₄, R₄, X₁₉, X₃₉, and X₄₉ are each         independently the same as described herein,     -   R_(1a) and R_(1b) are each independently the same as described         in connection with R₁,     -   R_(3a) and R_(3b) are each independently the same as described         in connection with R₃,     -   R_(4a) and R_(4b) are each independently the same as described         in connection with R₄,     -   R₁, R_(1a), R_(1b), R₃, R_(3a), R_(3b), R₄, R_(4a), and R_(4b)         may not be hydrogen, and     -   *, *′, and *″ each indicate a binding site to a neighboring         atom.

In one or more embodiments, the organometallic compound represented by Formula 1 may satisfy at least one of Condition 1-1 to Condition 4-1:

-   -   Condition 1-1     -   a moiety represented by

in Formula 1 is selected from groups represented by Formulae CZ1-1 to CZ1-7,

-   -   Condition 2-1     -   a moiety represented by

in Formula 1 is selected from groups represented by Formulae CZ2-1 to CZ2-6,

-   -   Condition 3-1     -   a moiety represented by

in Formula 1 is selected from groups represented by Formulae CZ3-1 to CZ3-6, and

-   -   Condition 4-1     -   a moiety represented

in by Formula 1 is selected from groups represented by Formulae CZ4-1 to CZ4-7.

For example, the organometallic compound represented by Formula 1 may be selected from Compounds 1 to 136, but embodiments of the present disclosure are not limited thereto:

The organometallic compound represented by Formula 1 has the same backbone as Formula 1 and satisfies at least one of Condition 1 to Condition 4 at the same time:

-   -   Condition 1     -   CY₁ in Formula 1 is a group represented by Formula CZ1, provided         that at least one of X₁₁ to X₁₇ in Formula CZ1 is each         independently N or C(CN),     -   Condition 2     -   at least one of X₂₁ to X₂₆ in Formula 1 is each independently N         or C(CN),     -   Condition 3     -   CY₃ in Formula 1 is a group represented by Formula CZ3, provided         that at least one of X₃₁ to X₃₆ in Formula CZ3 is each         independently N or C(CN), and     -   Condition 4     -   CY₄ in Formula 1 is a group represented by Formula CZ4, provided         that at least one of X₄₁ to X₄₇ in Formula CZ4 is each         independently N or C(CN).

Accordingly, the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO) energy levels of the organometallic compound represented by Formula 1 are adjustable, and in particular, the organometallic compound may have relatively low HOMO and LUMO energy levels (that is, large absolute values of HOMO and LUMO energy levels) and high triplet energy. Thus, an electronic device, for example, an organic light-emitting device, which includes the organometallic compound represented by Formula 1, may have improved efficiency and lifespan.

For example, a HOMO energy level, a LUMO energy level, and a triplet (T₁) energy level of Compounds 1, 2, 7, 17, 24, 25, and A were evaluated by using a density functional theory (DFT) method of a Gaussian program (B3LYP, structurally optimized at a level of 6-31G(d,p)). Evaluation results thereof are shown in Table 1.

TABLE 1 HOMO LUMO Compound energy level energy level No. (eV) (eV) T₁ energy level (eV) 1 −4.96 −1.89 2.68 2 −5.27 −1.70 2.79 7 −4.85 −1.52 2.78 17 −5.00 −1.67 2.75 24 −5.15 −1.69 2.88 25 −5.04 −1.65 2.72 A −4.64 −1.44 2.58

From Table 1, it has been determined that the organometallic compound represented by Formula 1 has such electrical characteristics that are suitable for use in an electronic device, for example, for use as a dopant for an organic light-emitting device.

Synthesis methods of the organometallic compound represented by Formula 1 may be recognizable by one of ordinary skill in the art by referring to Synthesis Examples provided below.

The organometallic compound represented by Formula 1 is suitable for use in an organic layer of an organic light-emitting device, for example, for use as a dopant in an emission layer of the organic layer. Thus, another aspect of the present description provides an organic light-emitting device that includes:

-   -   a first electrode;     -   a second electrode; and     -   an organic layer that is disposed between the first electrode         and the second electrode, wherein the organic layer includes an         emission layer and at least one organometallic compound         represented by Formula 1.

The organic light-emitting device may have, due to the inclusion of an organic layer including the organometallic compound represented by Formula 1, a low driving voltage, high efficiency, high power, high quantum efficiency, a long lifespan, a low roll-off ratio, and excellent color purity.

The organometallic compound of Formula 1 may be used between a pair of electrodes of an organic light-emitting device. For example, the organometallic compound represented by Formula 1 may be included in the emission layer. In this embodiment, the organometallic compound may act as a dopant, and the emission layer may further include a host (that is, an amount of the organometallic compound represented by Formula 1 is smaller than an amount of the host).

The expression “(an organic layer) includes at least one of organometallic compounds” as used herein may include an embodiment in which “(an organic layer) includes identical organometallic compounds represented by Formula 1” and an embodiment in which “(an organic layer) includes two or more different organometallic compounds represented by Formula 1.”

For example, the organic layer may include, as the organometallic compound, only Compound 1. In this embodiment, Compound 1 may be included in an emission layer of the organic light-emitting device. In one or more embodiments, the organic layer may include, as the organometallic compound, Compound 1 and Compound 2. In this embodiment, Compound 1 and Compound 2 may be included in an identical layer (for example, Compound 1 and Compound 2 may both be included in an emission layer).

The first electrode may be an anode, which is a hole injection electrode, and the second electrode may be a cathode, which is an electron injection electrode; or the first electrode may be a cathode, which is an electron injection electrode, and the second electrode may be an anode, which is a hole injection electrode.

In an embodiment, in the organic light-emitting device, the first electrode is an anode, and the second electrode is a cathode, and the organic layer further includes a hole transport region disposed between the first electrode and the emission layer and an electron transport region disposed between the emission layer and the second electrode, wherein the hole transport region includes a hole injection layer, a hole transport layer, an electron blocking layer, or any combination thereof, and wherein the electron transport region includes a hole blocking layer, an electron transport layer, an electron injection layer, or any combination thereof.

The term “organic layer” as used herein refers to a single layer and/or a plurality of layers between the first electrode and the second electrode of the organic light-emitting device. The “organic layer” may include, in addition to an organic compound, an organometallic complex including metal.

FIG. 1 is a schematic view of an organic light-emitting device 10 according to an embodiment. Hereinafter, the structure of an organic light-emitting device according to an embodiment and a method of manufacturing an organic light-emitting device according to an embodiment will be described in connection with FIG. 1. The organic light-emitting device 10 includes a first electrode 11, an organic layer 15, and a second electrode 19, which are sequentially stacked.

A substrate may be additionally disposed under the first electrode 11 or above the second electrode 19. For use as the substrate, any substrate that is used in general organic light-emitting devices may be used, and the substrate may be a glass substrate or a transparent plastic substrate, each having excellent mechanical strength, thermal stability, transparency, surface smoothness, ease of handling, and water resistance.

The first electrode 11 may be formed by depositing or sputtering a material for forming the first electrode 11 on the substrate. The first electrode 11 may be an anode. The material for forming the first electrode 11 may be selected from materials with a high work function to facilitate hole injection. The first electrode 11 may be a reflective electrode, a semi-transmissive electrode, or a transmissive electrode. The material for forming the first electrode may be, for example, indium tin oxide (ITO), indium zinc oxide (IZO), tin oxide (SnO₂), and zinc oxide (ZnO). In one or more embodiments, magnesium (Mg), aluminum (Al), aluminum-lithium (Al—Li), calcium (Ca), magnesium-indium (Mg—In), or magnesium-silver (Mg—Ag) may be used as the material for forming the first electrode.

The first electrode 11 may have a single-layered structure or a multi-layered structure including two or more layers. For example, the first electrode 11 may have a three-layered structure of ITO/Ag/ITO, but the structure of the first electrode 110 is not limited thereto.

The organic layer 15 is disposed on the first electrode 11.

The organic layer 15 may include a hole transport region, an emission layer, and an electron transport region.

The hole transport region may be disposed between the first electrode 11 and the emission layer.

The hole transport region may include a hole injection layer, a hole transport layer, an electron blocking layer, a buffer layer, or any combination thereof.

The hole transport region may include only either a hole injection layer or a hole transport layer. In one or more embodiments, the hole transport region may have a hole injection layer/hole transport layer structure or a hole injection layer/hole transport layer/electron blocking layer structure, which are sequentially stacked in this stated order from the first electrode 11.

A hole injection layer may be formed on the first electrode 11 by using one or more suitable methods selected from vacuum deposition, spin coating, casting, or Langmuir-Blodgett (LB) deposition.

When a hole injection layer is formed by vacuum deposition, the deposition conditions may vary according to a compound that is used to form the hole injection layer, and the structure and thermal characteristics of the hole injection layer. For example, the deposition conditions may include a deposition temperature of about 100° C. to about 500° C., a vacuum pressure of about 10⁻⁸ torr to about 10⁻³ torr, and a deposition rate of about 0.01 Angstroms per second (Å/sec) to about 100 Å/sec. However, the deposition conditions are not limited thereto.

When the hole injection layer is formed using spin coating, coating conditions may vary according to the material used to form the hole injection layer, and the structure and thermal properties of the hole injection layer. For example, a coating speed may be from about 2,000 revolutions per minute (rpm) to about 5,000 rpm, and a temperature at which a heat treatment is performed to remove a solvent after coating may be from about 80° C. to about 200° C. However, the coating conditions are not limited thereto.

Conditions for forming a hole transport layer and an electron blocking layer may be understood by referring to conditions for forming the hole injection layer.

The hole transport region may include at least one selected from m-MTDATA, TDATA, 2-TNATA, NPB, β-NPB, TPD, Spiro-TPD, Spiro-NPB, methylated-NPB, TAPC, HMTPD, 4,4′,4″-tris(N-carbazolyl)triphenylamine (TCTA), polyaniline/dodecylbenzene sulfonic acid (PANI/DBSA), poly(3,4-ethylenedioxythiophene)/poly(4-styrene sulfonate) (PEDOT/PSS), polyaniline/camphor sulfonic acid (PANI/CSA), polyaniline/poly(4-styrene sulfonate) (PANI/PSS), a compound represented by Formula 201 below, and a compound represented by Formula 202 below:

Ar₁₀₁ and Ar₁₀₂ in Formula 201 may each independently be selected from:

a phenylene group, a pentalenylene group, an indenylene group, a naphthylene group, an azulenylene group, a heptalenylene group, an acenaphthylene group, a fluorenylene group, a phenalenylene group, a phenanthrenylene group, an anthracenylene group, a fluoranthenylene group, a triphenylenylene group, a pyrenylene group, a chrysenylenylene group, a naphthacenylene group, a picenylene group, a perylenylene group, and a pentacenylene group; and

a phenylene group, a pentalenylene group, an indenylene group, a naphthylene group, an azulenylene group, a heptalenylene group, an acenaphthylene group, a fluorenylene group, a phenalenylene group, a phenanthrenylene group, an anthracenylene group, a fluoranthenylene group, a triphenylenylene group, a pyrenylene group, a chrysenylenylene group, a naphthacenylene group, a picenylene group, a perylenylene group, and a pentacenylene group, each substituted with at least one selected from deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl group, a C₁-C₆₀ alkoxy group, a C₃-C₁₀ cycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀ heterocycloalkyl group, a C₁-C₁₀ heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio group, a C₇-C₆₀ arylalkyl group, a C₁-C₆₀ heteroaryl group, a C₁-C₆₀ heteroaryloxy group, a C₁-C₆₀ heteroarylthio group, a C₂-C₆₀ heteroarylalkyl group, a monovalent non-aromatic condensed polycyclic group, and a monovalent non-aromatic condensed heteropolycyclic group.

In Formula 201, xa and xb may each independently be an integer from 0 to 5, or 0, 1, or 2. For example, xa is 1 and xb is 0, but xa and xb are not limited thereto.

R₁₀₁ to R₁₀₈, R₁₁₁ to R₁₁₉, and R₁₂₁ to R₁₂₄ in Formulae 201 and 202 may each independently be selected from:

hydrogen, deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C₁-C₁₀ alkyl group (for example, a methyl group, an ethyl group, a propyl group, a butyl group, a pentyl group, a hexyl group, and so on), or a C₁-C₁₀ alkoxy group (for example, a methoxy group, an ethoxy group, a propoxy group, a butoxy group, a pentoxy group, and so on);

a C₁-C₁₀ alkyl group or a C₁-C₁₀ alkoxy group, each substituted with at least one selected from deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, and a phosphoric acid group or a salt thereof;

a phenyl group, a naphthyl group, an anthracenyl group, a fluorenyl group, and a pyrenyl group; and

a phenyl group, a naphthyl group, an anthracenyl group, a fluorenyl group, and a pyrenyl group, each substituted with at least one selected from deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C₁-C₁₀ alkyl group, and a C₁-C₁₀ alkoxy group;

but embodiments of the present disclosure are not limited thereto.

R₁₀₉ in Formula 201 may be selected from:

a phenyl group, a naphthyl group, an anthracenyl group, and a pyridinyl group; and

a phenyl group, a naphthyl group, an anthracenyl group, and a pyridinyl group, each substituted with at least one selected from deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C₁-C₂₀ alkyl group, a C₁-C₂₀ alkoxy group, a phenyl group, a naphthyl group, an anthracenyl group, and a pyridinyl group.

According to an embodiment, the compound represented by Formula 201 may be represented by Formula 201 Å, but embodiments of the present disclosure are not limited thereto:

R₁₀₁, R₁₁₁, R₁₁₂, and R₁₀₉ in Formula 201A may be understood by referring to the description provided herein.

For example, the compound represented by Formula 201, and the compound represented by Formula 202 may include compounds HT1 to HT20 illustrated below, but are not limited thereto:

A thickness of the hole transport region may be in a range of about 100 Angstroms (Å) to about 10,000 Å, for example, about 100 Å to about 1,000 Å. When the hole transport region includes at least one of a hole injection layer and a hole transport layer, the thickness of the hole injection layer may be in a range of about 100 Å to about 10,000 Å, for example, about 100 Å to about 1,000 Å, and the thickness of the hole transport layer may be in a range of about 50 Å to about 2,000 Å, for example, about 100 Å to about 1,500 Å. While not wishing to be bound by theory, it is understood that when the thicknesses of the hole transport region, the hole injection layer, and the hole transport layer are within these ranges, satisfactory hole transporting characteristics may be obtained without a substantial increase in driving voltage.

The hole transport region may further include, in addition to these materials, a charge-generation material for the improvement of conductive properties. The charge-generation material may be homogeneously or non-homogeneously dispersed in the hole transport region.

The charge-generation material may be, for example, a p-dopant. The p-dopant may be one selected from a quinone derivative, a metal oxide, and a cyano group-containing compound, but embodiments of the present disclosure are not limited thereto. Non-limiting examples of the p-dopant are a quinone derivative, such as tetracyanoquinonedimethane (TCNQ) or 2,3,5,6-tetrafluoro-tetracyano-1,4-benzoquinonedimethane (F4-TCNQ); a metal oxide, such as a tungsten oxide or a molybdenium oxide; and a cyano group-containing compound, such as Compound HT-D1 below, but are not limited thereto:

The hole transport region may include a buffer layer.

Also, the buffer layer may compensate for an optical resonance distance according to a wavelength of light emitted from the emission layer, and thus, efficiency of a formed organic light-emitting device may be improved.

Then, an emission layer may be formed on the hole transport region by vacuum deposition, spin coating, casting, LB deposition, or the like. When the emission layer is formed by vacuum deposition or spin coating, the deposition or coating conditions may be similar to those applied in forming the hole injection layer although the deposition or coating conditions may vary according to a compound that is used to form the emission layer.

Meanwhile, when the hole transport region includes an electron blocking layer, a material for the electron blocking layer may be selected from materials for the hole transport region described above and materials for a host to be explained later. However, the material for the electron blocking layer is not limited thereto. For example, when the hole transport region includes an electron blocking layer, a material for the electron blocking layer may be mCP, which will be explained later.

The emission layer may include a host and a dopant, and the dopant may include the organometallic compound represented by Formula 1.

The host may include at least one selected from TPBi, TBADN, ADN (also referred to as “DNA”), CBP, CDBP, TCP, mCP, Compound H50, and Compound H51:

In one or more embodiments, the host may further include a compound represented by Formula 301 below:

In Formula 301, Ar₁₁₁ and Ar₁₁₂ may each independently be selected from:

a phenylene group, a naphthylene group, a phenanthrenylene group, and a pyrenylene group; and

a phenylene group, a naphthylene group, a phenanthrenylene group, and a pyrenylene group, each substituted with at least one selected from a phenyl group, a naphthyl group, and an anthracenyl group.

In Formula 301, Ar₁₁₃ to Ar₁₁₆ may each independently be selected from:

a C₁-C₁₀ alkyl group, a phenyl group, a naphthyl group, a phenanthrenyl group, and a pyrenyl group; and

a phenyl group, a naphthyl group, a phenanthrenyl group, and a pyrenyl group, each substituted with at least one selected from a phenyl group, a naphthyl group, and an anthracenyl group.

In Formula 301, g, h, i, and j may each independently be an integer from 0 to 4, and for example, may be 0, 1, or 2.

In Formula 301, Ar₁₁₃ to Ar₁₁₆ may each independently be selected from:

a C₁-C₁₀ alkyl group substituted with at least one selected from a phenyl group, a naphthyl group, and an anthracenyl group;

a phenyl group, a naphthyl group, an anthracenyl group, a pyrenyl group, a phenanthrenyl group, and a fluorenyl group;

a phenyl group, a naphthyl group, an anthracenyl group, a pyrenyl group, a phenanthrenyl group, and a fluorenyl group, each substituted with at least one selected from deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl group, a C₁-C₆₀ alkoxy group, a phenyl group, a naphthyl group, an anthracenyl group, a pyrenyl group, a phenanthrenyl group, and a fluorenyl group; and

but embodiments of the present disclosure are not limited thereto.

In one or more embodiments, the host may include a compound represented by Formula 302 below:

Ar₁₂₂ to Ar₁₂₅ in Formula 302 are the same as described in detail in connection with Ar₁₁₃ in Formula 301.

Ar₁₂₆ and Ar₁₂₇ in Formula 302 may each independently be a C₁-C₁₀ alkyl group (for example, a methyl group, an ethyl group, or a propyl group).

k and l in Formula 302 may each independently be an integer from 0 to 4. For example, k and l may be 0, 1, or 2.

The compound represented by Formula 301 and the compound represented by Formula 302 may include Compounds H1 to H42 illustrated below, but are not limited thereto:

When the organic light-emitting device is a full-color organic light-emitting device, the emission layer may be patterned into a red emission layer, a green emission layer, and a blue emission layer. In one or more embodiments, due to a stacked structure including a red emission layer, a green emission layer, and/or a blue emission layer, the emission layer may emit white light.

When the emission layer includes a host and dopant, an amount of the dopant may be typically in a range of about 0.01 parts by weight to about 15 parts by weight based on 100 parts by weight of the host, but embodiments of the present disclosure are not limited thereto.

A thickness of the emission layer may be in a range of about 100 Å to about 1,000 Å, for example, about 200 Å to about 600 Å. While not wishing to be bound by theory, it is understood that when the thickness of the emission layer is within this range, excellent light-emission characteristics may be obtained without a substantial increase in driving voltage.

Then, an electron transport region may be disposed on the emission layer.

The electron transport region may include a hole blocking layer, an electron transport layer, an electron injection layer, or any combination thereof.

For example, the electron transport region may have a hole blocking layer/electron transport layer/electron injection layer structure or an electron transport layer/electron injection layer structure, but the structure of the electron transport region is not limited thereto. The electron transport layer may have a single-layered structure or a multi-layered structure including two or more different materials.

Conditions for forming the hole blocking layer, the electron transport layer, and the electron injection layer which constitute the electron transport region may be understood by referring to the conditions for forming the hole injection layer.

When the electron transport region includes a hole blocking layer, the hole blocking layer may include, for example, at least one of BCP, Bphen, and BAlq but embodiments of the present disclosure are not limited thereto:

A thickness of the hole blocking layer may be in a range of about 20 Å to about 1,000 Å, for example, about 30 Å to about 300 Å. While not wishing to be bound by theory, it is understood that when the thickness of the hole blocking layer is within these ranges, the hole blocking layer may have improved hole blocking ability without a substantial increase in driving voltage.

The electron transport layer may include at least one selected from BCP, Bphen, Alq₃, BAlq, TAZ, and NTAZ:

In one or more embodiments, the electron transport layer may include at least one of ET1 and ET2, but are not limited thereto:

A thickness of the electron transport layer may be in a range of about 100 Å to about 1,000 Å, for example, about 150 Å to about 500 Å. When the thickness of the electron transport layer is within the range described above, the electron transport layer may have satisfactory electron transport characteristics without a substantial increase in driving voltage.

Also, the electron transport layer may further include, in addition to the materials described above, a metal-containing material.

The metal-containing material may include a Li complex. The Li complex may include, for example, Compound ET-D1 (lithium 8-hydroxyquinolate, LiQ) or ET-D2:

The electron transport region may include an electron injection layer that promotes flow of electrons from the second electrode 19 thereinto.

The electron injection layer may include at least one selected from LiF, NaCl, CsF, Li₂O, and BaO.

A thickness of the electron injection layer may be in a range of about 1 Å to about 100 Å, for example, about 3 Å to about 90 Å. While not wishing to be bound by theory, it is understood that when the thickness of the electron injection layer is within the range described above, the electron injection layer may have satisfactory electron injection characteristics without a substantial increase in driving voltage.

The second electrode 19 is disposed on the organic layer 15. The second electrode 19 may be a cathode. A material for forming the second electrode 19 may be selected from metal, an alloy, an electrically conductive compound, and a combination thereof, which have a relatively low work function. For example, lithium (Li), magnesium (Mg), aluminum (Al), aluminum-lithium (Al—Li), calcium (Ca), magnesium-indium (Mg—In), or magnesium-silver (Mg—Ag) may be used as a material for forming the second electrode 19. In one or more embodiments, to manufacture a top-emission type light-emitting device, a transmissive electrode formed using ITO or IZO may be used as the second electrode 19.

Hereinbefore, the organic light-emitting device has been described with reference to FIG. 1, but embodiments of the present disclosure are not limited thereto.

Another aspect of the present disclosure provides a diagnostic composition including at least one organometallic compound represented by Formula 1.

The organometallic compound represented by Formula 1 provides high luminescent efficiency. Accordingly, a diagnostic composition including the organometallic compound may have high diagnostic efficiency.

The diagnostic composition may be used in various applications including a diagnosis kit, a diagnosis reagent, a biosensor, and a biomarker.

The term “C₁-C₆₀ alkyl group” as used herein refers to a linear or branched saturated aliphatic hydrocarbon monovalent group having 1 to 60 carbon atoms, and non-limiting examples thereof include a methyl group, an ethyl group, a propyl group, an iso-butyl group, a sec-butyl group, a tert-butyl group, a pentyl group, an iso-amyl group, and a hexyl group. The term “C₁-C₆₀ alkylene group” as used herein refers to a divalent group having the same structure as the C₁-C₆₀ alkyl group.

The term “C₁-C₆₀ alkoxy group” as used herein refers to a monovalent group represented by —OA₁₀₁ (wherein A₁₀₁ is the C₁-C₆₀ alkyl group), and non-limiting examples thereof include a methoxy group, an ethoxy group, and an iso-propyloxy group.

The term “C₂-C₆₀ alkenyl group” as used herein refers to a hydrocarbon group formed by including at least one carbon-carbon double bond in the middle or at the terminus of the C₂-C₆₀ alkyl group, and examples thereof include an ethenyl group, a propenyl group, and a butenyl group. The term “C₂-C₆₀ alkenylene group” as used herein refers to a divalent group having the same structure as the C₂-C₆₀ alkenyl group.

The term “C₂-C₆₀ alkynyl group” as used herein refers to a hydrocarbon group formed by including at least one carbon-carbon triple bond in the middle or at the terminus of the C₂-C₆₀ alkyl group, and examples thereof include an ethynyl group, and a propynyl group. The term “C₂-C₆₀ alkynylene group” as used herein refers to a divalent group having the same structure as the C₂-C₆₀ alkynyl group.

The term “C₃-C₁₀ cycloalkyl group” as used herein refers to a monovalent saturated hydrocarbon monocyclic group having 3 to 10 carbon atoms, and non-limiting examples thereof include a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group, and a cycloheptyl group. The term “C₃-C₁₀ cycloalkylene group” as used herein refers to a divalent group having the same structure as the C₃-C₁₀ cycloalkyl group.

The term “C₁-C₁₀ heterocycloalkyl group” as used herein refers to a monovalent saturated monocyclic group having at least one heteroatom selected from N, O, P, Si and S as a ring-forming atom and 1 to 10 carbon atoms, and non-limiting examples thereof include a tetrahydrofuranyl group, and a tetrahydrothiophenyl group. The term “C₁-C₁₀ heterocycloalkylene group” as used herein refers to a divalent group having the same structure as the C₁-C₁₀ heterocycloalkyl group.

The term “C₃-C₁₀ cycloalkenyl group” as used herein refers to a monovalent monocyclic group that has 3 to 10 carbon atoms and at least one carbon-carbon double bond in the ring thereof and that has no aromaticity, and non-limiting examples thereof include a cyclopentenyl group, a cyclohexenyl group, and a cycloheptenyl group. The term “C₃-C₁₀ cycloalkenylene group” as used herein refers to a divalent group having the same structure as the C₃-C₁₀ cycloalkenyl group.

The term “C₁-C₁₀ heterocycloalkenyl group” as used herein refers to a monovalent monocyclic group that has at least one heteroatom selected from N, O, P, Si, and S as a ring-forming atom, 1 to 10 carbon atoms, and at least one carbon-carbon double bond in its ring. Examples of the C₁-C₁₀ heterocycloalkenyl group are a 2,3-dihydrofuranyl group, and a 2,3-dihydrothiophenyl group. The term “C₁-C₁₀ heterocycloalkenylene group” as used herein refers to a divalent group having the same structure as the C₁-C₁₀ heterocycloalkenyl group.

The term “C₆-C₆₀ aryl group” as used herein refers to a monovalent group having a carbocyclic aromatic system having 6 to 60 carbon atoms, and the term “C₆-C₆₀ arylene group” as used herein refers to a divalent group having a carbocyclic aromatic system having 6 to 60 carbon atoms. Non-limiting examples of the C₆-C₆₀ aryl group include a phenyl group, a naphthyl group, an anthracenyl group, a phenanthrenyl group, a pyrenyl group, and a chrysenyl group. When the C₆-C₆₀ aryl group and the C₆-C₆₀ arylene group each include two or more rings, the rings may be fused to each other.

The term “C₁-C₆₀ heteroaryl group” as used herein refers to a monovalent group having a carbocyclic aromatic system that has at least one heteroatom selected from N, O, P, Si, and S as a ring-forming atom, and 1 to 60 carbon atoms. The term “C₁-C₆₀ heteroarylene group” as used herein refers to a divalent group having a carbocyclic aromatic system that has at least one heteroatom selected from N, O, P, and S as a ring-forming atom, and 1 to 60 carbon atoms. Non-limiting examples of the C₁-C₆₀ heteroaryl group include a pyridinyl group, a pyrimidinyl group, a pyrazinyl group, a pyridazinyl group, a triazinyl group, a quinolinyl group, and an isoquinolinyl group. When the C₁-C₆₀ heteroaryl group and the C₁-C₆₀ heteroarylene group each include two or more rings, the rings may be fused to each other.

The term “C₆-C₆₀ aryloxy group” as used herein indicates —OA₁₀₂ (wherein A₁₀₂ is the C₆-C₆₀ aryl group), the term “C₆-C₆₀ arylthio group” as used herein indicates —SA₁₀₃ (wherein A₁₀₃ is the C₆-C₆₀ aryl group), and the term “C₇-C₆₀ arylalkyl group” as used herein indicates -A₁₀₄A₁₀₅ (wherein A₁₀₄ is the C₆-C₅₉ aryl group and A₁₀₅ is the C₁-C₅₃ alkyl group).

The term “C₁-C₆₀ heteroaryloxy group” as used herein refers to —OA₁₀₆ (wherein A₁₀₆ is the C₁-C₆₀ heteroaryl group), and the term “C₁-C₆₀ heteroarylthio group” as used herein indicates —SA₁₀₇ (wherein A₁₀₇ is the C₁-C₆₀ heteroaryl group).

The term “C₂-C₆₀ heteroarylalkyl group” as used herein refers to -A₁₀₈A₁₀₉ (A₁₀₉ is a C₁-C₅₉ heteroaryl group, and A₁₀₈ is a C₁-C₅₈ alkylene group).

The term “monovalent non-aromatic condensed polycyclic group” as used herein refers to a monovalent group (for example, having 8 to 60 carbon atoms) having two or more rings condensed to each other, only carbon atoms as ring-forming atoms, and no aromaticity in its entire molecular structure. Examples of the monovalent non-aromatic condensed polycyclic group include a fluorenyl group. The term “divalent non-aromatic condensed polycyclic group,” as used herein, refers to a divalent group having the same structure as the monovalent non-aromatic condensed polycyclic group.

The term “monovalent non-aromatic condensed heteropolycyclic group” as used herein refers to a monovalent group (for example, having 2 to 60 carbon atoms) having two or more rings condensed to each other, a heteroatom selected from N, O, P, Si, and S, other than carbon atoms, as a ring-forming atom, and no aromaticity in its entire molecular structure. Non-limiting examples of the monovalent non-aromatic condensed heteropolycyclic group include a carbazolyl group. The term “divalent non-aromatic condensed heteropolycyclic group” as used herein refers to a divalent group having the same structure as the monovalent non-aromatic condensed heteropolycyclic group.

The term “C₅-C₃₀ carbocyclic group” as used herein refers to a saturated or unsaturated cyclic group having, as a ring-forming atom, 5 to 30 carbon atoms only. The C₅-C₃₀ carbocyclic group may be a monocyclic group or a polycyclic group.

The term “C₁-C₃₀ heterocyclic group” as used herein refers to a saturated or unsaturated cyclic group having, as a ring-forming atom, at least one heteroatom selected from N, O, Si, P, and S other than 1 to 30 carbon atoms. The C₁-C₃₀ heterocyclic group may be a monocyclic group or a polycyclic group.

At least one substituent of the selected substituted C₅-C₃₀ carbocyclic group, the substituted C₂-C₃₀ heterocyclic group, the substituted C₁-C₆₀ alkyl group, the substituted C₂-C₆₀ alkenyl group, the substituted C₂-C₆₀ alkynyl group, the substituted C₁-C₆₀ alkoxy group, the substituted C₃-C₁₀ cycloalkyl group, the substituted C₁-C₁₀ heterocycloalkyl group, the substituted C₃-C₁₀ cycloalkenyl group, the substituted C₁-C₁₀ heterocycloalkenyl group, the substituted C₆-C₆₀ aryl group, the substituted C₆-C₆₀ aryloxy group, the substituted C₆-C₆₀ arylthio group, the substituted C₇-C₆₀ arylalkyl group, the substituted C₁-C₆₀ heteroaryl group, the substituted C₁-C₆₀ heteroaryloxy group, the substituted C₁-C₆₀ heteroarylthio group, the substituted C₂-C₆₀ heteroarylalkyl group, the substituted monovalent non-aromatic condensed polycyclic group, and the substituted monovalent non-aromatic condensed heteropolycyclic group may be selected from:

deuterium, —F, —Cl, —Br, —I, —CD₃, —CD₂H, —CDH₂, —CF₃, —CF₂H, —CFH₂, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl group, and a C₁-C₆₀ alkoxy group;

a C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl group, and a C₁-C₆₀ alkoxy group, each substituted with at least one selected from deuterium, —F, —Cl, —Br, —I, —CD₃, —CD₂H, —CDH₂, —CF₃, —CF₂H, —CFH₂, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C₃-C₁₀ cycloalkyl group, a C₁-C₁₀ heterocycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀ heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio group, a C₇-C₆₀ arylalkyl group, a C₁-C₆₀ heteroaryl group, a C₁-C₆₀ heteroaryloxy group, a C₁-C₆₀ heteroarylthio group, a C₂-C₆₀ heteroarylalkyl group, a monovalent non-aromatic condensed polycyclic group, a monovalent non-aromatic condensed heteropolycyclic group, —N(Q₁₁)(Q₁₂), —Si(Q₁₃)(Q₁₄)(Q₁₅), —B(Q₁₆)(Q₁₇), and —P(═O)(Q₁₈)(Q₁₉);

a C₃-C₁₀ cycloalkyl group, a C₁-C₁₀ heterocycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀ heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio group, a C₇-C₆₀ arylalkyl group, a C₁-C₆₀ heteroaryl group, a C₁-C₆₀ heteroaryloxy group, a C₁-C₆₀ heteroarylthio group, a C₂-C₆₀ heteroarylalkyl group, a monovalent non-aromatic condensed polycyclic group, and a monovalent non-aromatic condensed heteropolycyclic group;

a C₃-C₁₀ cycloalkyl group, a C₁-C₁₀ heterocycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀ heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio group, a C₇-C₆₀ arylalkyl group, a C₁-C₆₀ heteroaryl group, a C₁-C₆₀ heteroaryloxy group, a C₁-C₆₀ heteroarylthio group, a C₂-C₆₀ heteroarylalkyl group, a monovalent non-aromatic condensed polycyclic group, and a monovalent non-aromatic condensed heteropolycyclic group, each substituted with at least one selected from deuterium, —F, —Cl, —Br, —I, —CD₃, —CD₂H, —CDH₂, —CF₃, —CF₂H, —CFH₂, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl group, a C₁-C₆₀ alkoxy group, a C₃-C₁₀ cycloalkyl group, a C₁-C₁₀ heterocycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀ heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio group, a C₇-C₆₀ arylalkyl group, a C₁-C₆₀ heteroaryl group, a C₁-C₆₀ heteroaryloxy group, a C₁-C₆₀ heteroarylthio group, a C₂-C₆₀ heteroarylalkyl group, a monovalent non-aromatic condensed polycyclic group, a monovalent non-aromatic condensed heteropolycyclic group, —N(Q₂₁)(Q₂₂), —Si(Q₂₃)(Q₂₄)(Q₂₅), —B(Q₂₆)(Q₂₇), and —P(═O)(Q₂₈)(Q₂₉); and

—N(Q₃₁)(Q₃₂), —Si(Q₃₃)(Q₃₄)(Q₃₅), —B(Q₃₆)(Q₃₇), and —P(═O)(Q₃₈)(Q₃₉), and

Q₁ to Q₉, Q₁₁ to Q₁₉, Q₂₁ to Q₂₉, and Q₃₁ to Q₃₉ may each independently be selected from hydrogen, deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl group, a C₁-C₆₀ alkoxy group, a C₃-C₁₀ cycloalkyl group, a C₁-C₁₀ heterocycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀ heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₆-C₆₀ aryl group substituted with at least one selected from a C₁-C₆₀ alkyl group, and a C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio group, a C₇-C₆₀ arylalkyl group, a C₁-C₆₀ heteroaryl group, a C₁-C₆₀ heteroaryloxy group, a C₁-C₆₀ heteroarylthio group, a C₂-C₆₀ heteroarylalkyl group, a monovalent non-aromatic condensed polycyclic group, and a monovalent non-aromatic condensed heteropolycyclic group.

Hereinafter, a compound and an organic light-emitting device according to embodiments are described in detail with reference to Synthesis Examples and Examples. However, the organic light-emitting device is not limited thereto. The wording “B was used instead of A” used in describing Synthesis Examples means that an amount of A used was identical to an amount of B used, in terms of molar equivalents.

EXAMPLES Synthesis Example 1: Synthesis of Compound 1

Synthesis of Ligand 1-3

28.7 millimoles (mmol) (10 grams, g) of 3,3′-oxybis(9H-carbazole), 86.1 mmol (13.6 g) of 2-bromopyridine, 28.7 mmol (5.4 g) of CuI, 115 mmol (24.4 g) of K₃PO₄, and 57.4 mmol (6.5 g) of 1,2-diaminocyclohexane were added to 250 milliliters (mL) of dioxane, and the resultant mixture was refluxed at a temperature of 120° C. for 12 hours. A reaction mixture obtained therefrom was cooled, and an organic layer was extracted by using a mixture of ethyl acetate and water. The extracted organic layer was washed with water three times and dried by using magnesium sulfate, and a solvent was removed therefrom under reduced pressure. The crude product was purified by silica gel column chromatography (eluent: dichloromethane and hexane) to obtain Ligand 1-3 (yield: 80%).

MALDI-TOF (m/z): 502.33 [M]⁺.

Synthesis of Ligand 1-2

Methylene chloride (MC) and 22.9 mmol (11.5 g) of Ligand 1-3 were mixed, and 23 mmol (1 equivalent (equiv.), 4.1 g) of n-bromosuccinimide was added thereto. The resultant mixture was refluxed at a temperature of 40° C. for 12 hours. A reaction mixture obtained therefrom was cooled, and an organic layer was extracted by using a mixture of ethyl acetate and water. The extracted organic layer was washed with water three times and dried by using magnesium sulfate, and a solvent was removed therefrom under reduced pressure. The obtained crude product (Ligand 1-2) was used in a subsequent reaction.

MALDI-TOF (m/z): 581.23 [M]⁺.

Synthesis of Ligand 1-1

22.9 mmol (13.3 g) of Ligand 1-2 was added to a mixture of 22.9 mmol (1 equiv.) of copper cyanide (CuCN) and 90 mL of dimethylformamide (DMF). The resultant mixture was refluxed at a temperature of 150° C. for 12 hours. A reaction mixture obtained therefrom was cooled, and an organic layer was extracted by using a mixture of ethyl acetate and water. The extracted organic layer was washed with water three times and dried by using magnesium sulfate, and a solvent was removed therefrom under reduced pressure. The crude product was purified by silica gel column chromatography (eluent: ethyl acetate and hexane) to obtain Ligand 1-1 (yield: 30%).

MALDI-TOF (m/z): 527.37 [M]⁺.

Synthesis of Compound 1

1.9 mmol (0.9 g) of PtCl₂(NCPh)₂ and 1.9 mmol (1 g) of Ligand 1-1 were added to 10 mL of benzonitrile. The resultant mixture was refluxed in a nitrogen atmosphere for 5 hours. After the reaction was completed, the resultant mixture was cooled to room temperature and 50 mL of distilled water was added to a reaction vessel. After a solid obtained therefrom was filtered, washed with distilled water, and then dried, the crude product was purified by silica gel column chromatography (eluent: dichloromethane and hexane) to obtain Compound 1 (yield: 23%).

MALDI-TOF (m/z): 720.10 [M]⁺.

Synthesis Example 2: Synthesis of Compound 2

Synthesis of Ligand 2-2

Ligand 2-2 was synthesized in the same manner as Ligand 1-2 in Synthesis Example 1, except that an amount of n-bromosuccinimide used was changed to 2 equiv.

MALDI-TOF (m/z): 660.10 [M]⁺.

Synthesis of Ligand 2-1

Ligand 2-1 (yield: 27%) was synthesized in the same manner as Ligand 1-1 in Synthesis Example 1, except that an amount of copper cyanide (CuCN) used was changed to 2 equiv.

MALDI-TOF (m/z): 552.17 [M]⁺.

Synthesis of Compound 2

Compound 2 (yield: 25%) was synthesized in the same manner as Compound 1 in Synthesis Example 1, except that Ligand 2-1 was used instead of Ligand 1-1.

MALDI-TOF (m/z): 745.01[M]⁺.

Synthesis Example 3: Synthesis of Compound 7

Synthesis of Ligand 7-3

Ligand 7-3 (yield: 85%) was synthesized in the same manner as Ligand 1-3 in Synthesis Example 1, except that 2-bromo-4-(tert-butyl)pyridine was used instead of 2-bromopyridine.

MALDI-TOF (m/z): 612.65 [M]⁺.

Synthesis of Ligand 7-2

Ligand 7-2 (yield: 85%) was synthesized in the same manner as Ligand 1-2 in Synthesis Example 1, except that Ligand 7-3 was used instead of Ligand 1-3.

Synthesis of Ligand 7-1

Ligand 7-1 (yield: 27%) was synthesized in the same manner as used to synthesize Ligand 1-1 in Synthesis Example 1, except that Ligand 7-2 was used instead of Ligand 1-2.

MALDI-TOF (m/z): 639.32 [M]⁺.

Synthesis of Compound 7

Compound 7 (yield: 27%) was synthesized in the same manner as used to synthesize Compound 1 in Synthesis Example 1, except that Ligand 7-1 was used instead of Ligand 1-1.

MALDI-TOF (m/z): 832.54 [M]⁺.

Synthesis Example 4: Synthesis of Compound 24

Synthesis of Ligand 24-2

Ligand 24-2 was synthesized in the same manner as Ligand 7-2 in Synthesis Example 3, except that an amount of n-bromosuccinimide used was changed to 2 equiv.

Synthesis of Ligand 24-1

Ligand 24-1 (yield: 23%) was synthesized in the same manner as Ligand 7-1 in Synthesis Example 3, except that an amount of copper cyanide (CuCN) used was changed to 2 equiv.

MALDI-TOF (m/z): 662.90 [M]⁺.

Synthesis of Compound 24

Compound 24 (yield: 23%) was synthesized in the same manner as Compound 7 in Synthesis Example 3, except that Ligand 24-1 was used instead of Ligand 7-1.

MALDI-TOF (m/z): 857.18 [M]⁺.

Synthesis Example 5: Synthesis of Compound 25

Synthesis of Ligand 25-1

Ligand 25-1 (yield: 60%) was synthesized in the same manner as Ligand 1-3 in Synthesis Example 1, except that 7,7′-oxybis(9H-pyrido[3,4-b]indole) was used instead of 3,3′-oxybis(9H-carbazole).

MALDI-TOF (m/z): 505.14 [M]⁺.

Synthesis of Compound 25

2.0 mmol (0.9 g) of PtCl₂(NCPh)₂, 2.0 mmol (1 g) of Ligand 25-1, and 10 mL of benzonitrile were mixed and refluxed in a nitrogen atmosphere for 5 hours. After the reaction was completed, the resultant mixture was cooled to room temperature and 50 mL of distilled water was added to a reaction vessel. A solid obtained therefrom was filtered and washed by using ethyl acetate to obtain Compound 25 (yield: 18%).

MALDI-TOF (m/z): 697.84 [M]⁺.

Evaluation Example 1: Evaluation of PL Spectrum

After Compound 1 was diluted at a concentration of 10 millimolar (mM) in toluene, a photoluminescence (PL) spectrum thereof was measured at room temperature by using an ISC PC1 spectrofluorometer equipped with a xenon lamp. This process was repeated on Compounds 2, 7, A, 7, 24, and B. Results thereof are shown in Table 2 and FIG. 2.

TABLE 2 Maximum emission Compound No. wavelength (nm) FWHM (nm) 1 489 31 2 461 76 A 511 95 7 442, 465 59 24  434, 462 43 B 480 89

Referring to Table 2 and FIG. 2, it has been determined that Compounds 1 and 2 can emit light relatively shifted to a blue light-emitting area and having an improved (that is, reduced) full width at half maximum (FWHM), as compared with Compound A, and Compounds 7 and 24 can emit light relatively shifted to a blue light-emitting area and having an improved (that is, reduced) FWHM, as compared with Compound B.

Evaluation Example 2: Evaluation of HOMO, LUMO, and T1 Energy Levels

HOMO and LUMO energy levels of Compounds 7, A, and B and T₁ energy levels of Compounds 1, 2, 7, 24, A, and B were measured according to methods described in Table 3, and results thereof are shown in Table 4:

TABLE 3 HOMO energy A voltage-current (V-A) graph of each Compound was obtained by level evaluation using a cyclic voltammetry (CV) (electrolyte: 0.1 molar (M) method Bu₄NPF₆/solvent: CH₂Cl₂/electrode: 3-electrode system (working electrode: Pt disc (1 millimeter (mm) diameter), reference electrode: Pt wire, and auxiliary electrode: Pt wire)), and the HOMO energy level of each Compound was calculated from an oxidation onset of the V-A graph. LUMO energy Each compound was diluted at a concentration of 1 × 10⁻⁵ M in level evaluation CHCl₃, and an UV absorption spectrum thereof was measured at method room temperature by using a Shimadzu UV-350 spectrometer, and a LUMO energy level thereof was calculated by using an optical band gap (Eg) and HOMO energy levels from an edge of the absorption spectrum. T₁ energy level After a mixture of toluene and each Compound (1 milligram (mg) evaluation of each Compound was dissolved in 3 cubic centimeters (cc) of method toluene) was added to a quartz cell and then added to liquid nitrogen (77 Kelvin, K), a photoluminescence spectrum was measured by using a photoluminescence measurement apparatus. The T₁ energy level was calculated by analyzing peaks alone observed only at a low temperature through comparison between the photoluminescence spectrum and a general room-temperature photoluminescence spectrum.

TABLE 4 Compound No. HOMO (eV) LUMO (eV) T₁ (eV) 1 — — 2.69 2 — — 2.54 A −5.17 −2.75 2.42 7 −5.41 −2.60 2.81 24  — — 2.86 B −5.18 −2.60 2.58

Referring to Table 4, it has been determined that Compound 7 has a lower HOMO energy level (that is, a large absolute value of a HOMO energy level) than Compounds A and B, Compounds 1 and 2 has a higher T₁ energy level than Compound A, and Compounds 7 and 24 has a higher T₁ energy level than Compound B.

Example 1

As an anode, a glass substrate, on which ITO/Ag/ITO were respectively deposited to thicknesses of 70 Å/1,000 Å/70 Å, was cut to a size of 50 mm×50 mm×0.5 mm (mm=millimeters), sonicated with iso-propyl alcohol and pure water each for 5 minutes, and then cleaned by exposure ultraviolet (UV) rays for 30 minutes. Then, the glass substrate was provided to a vacuum deposition apparatus.

2-TNATA was deposited on the anode to form a hole injection layer having a thickness of 600 Å, and 4,4′-bis[N-(1-naphthyl)-N-phenylamino]biphenyl (NPB) was deposited on the hole injection layer to form a hole transport layer having a thickness of 1,350 Å.

CBP (host) and Compound 1 (dopant) was co-deposited on the hole transport layer at a weight ratio of 94:6 to form an emission layer having a thickness of 400 Å, and BCP was deposited on the emission layer to form a hole blocking layer having a thickness of 50 Å. Then, Alq₃ was deposited on the hole blocking layer to form an electron transport layer having a thickness of 350 Å, LiF was deposited on the electron transport layer to form an electron injection layer having a thickness of 10 Å, and MgAg was deposited on the electron injection layer at a weight ratio of 90:10 to form a cathode having a thickness of 120 Å, thereby completing the manufacture of an organic light-emitting device.

Examples 2 to 4

Organic light-emitting devices were manufactured in the same manner as in Example 1, except that Compounds 2, 7, and 24 were each used instead of Compound 1 as a dopant in forming an emission layer.

Evaluation Example 3: Evaluation on Characteristics of Organic Light-Emitting Devices

The driving voltage, emission efficiency, quantum emission efficiency, and roll-off ratio of the organic light-emitting device manufactured according to Example 3 were evaluated by using a current-voltage meter (Keithley 2400) and a luminance meter (Minolta Cs-1000 Å), and results thereof are shown in Table 5. The roll-off ratio was calculated by using Equation 20. Roll off={1−(efficiency (at 9000 nit)/maximum emission efficiency)}×100%  Equation 20

TABLE 5 Dopant Driving Emission Quantum Roll-off Example compound voltage efficiency emission ratio No. No. (V) (cd/A) efficiency (%) (%) Example 7 5.6 15.4 5.5 17.5 3

Referring to Table 5, it has been determined that the organic light-emitting device of Example 3 has excellent driving voltage, emission efficiency, quantum emission efficiency, and roll-off ratio characteristics.

As described above, the organometallic compounds according to embodiments of the present disclosure have excellent electrical characteristics and thermal stability, and accordingly, organic light-emitting devices including such organometallic compounds may have excellent driving voltage, efficiency, power, color purity, and lifespan characteristics. Also, due to excellent phosphorescent luminescence characteristics, such organometallic compounds may provide a diagnostic composition having high diagnostic efficiency.

It should be understood that embodiments described herein should be considered in a descriptive sense only and not for purposes of limitation. Descriptions of features or aspects within each embodiment should typically be considered as available for other similar features or aspects in other embodiments.

While one or more embodiments have been described with reference to the figures, it will be understood by those of ordinary skill in the art that various changes in form and details may be made therein without departing from the spirit and scope of the present description as defined by the following claims. 

What is claimed is:
 1. An organometallic compound represented by Formula 1:

wherein, in Formulae 1, CZ1, CZ3, and CZ4, M is selected from a first-row transition metal of the Periodic Table of Elements, a second-row transition metal of the Periodic Table of Elements, and a third-row transition metal of the Periodic Table of Elements, X₁ to X₄ are each independently C or N, two bonds selected from a bond between X₁ and M, a bond between X₂ and M, a bond between X₃ and M, and a bond between X₄ and M are each a coordinate bond, and the others thereof are each a covalent bond, Y₂ to Y₅ are each independently C or N, Y₁ and Y₆ are each independently C, N, O, Si, or S, a bond between X₁ and Y₁, a bond between X₁ and Y₂, a bond between X₃ and Y₃, a bond between X₃ and Y₄, a bond between X₄ and Y₅, and a bond between X₄ and Y₆ are each a chemical bond that links the corresponding atoms, CY₁ is selected from a C₅-C₃₀ carbocyclic group, a C₁-C₃₀ heterocyclic group, and a group represented by Formula CZ1, CY₃ is selected from a C₅-C₃₀ carbocyclic group, a C₁-C₃₀ heterocyclic group, and a group represented by Formula CZ3, CY₄ is selected from a C₅-C₃₀ carbocyclic group, a C₁-C₃₀ heterocyclic group, and a group represented by Formula CZ4, T₁ to T₃ are each independently selected from *—N[(L₅)_(b5)-(R₅)]—*′, *—B(R₅)—*′, *—P(R₅)—*′, *—C(R₅)(R₆)—*′, *—Si(R₅)(R₆)—*′, *—Ge(R₅)(R₆)—*′, *—S—*′, *—Se—*′, *—O—*′, *—C(═O)—*′, *—S(═O)—*′, *—S(═O)₂—*′, *—C(R₅)=*′, *═C(R₅)—*′, *—C(R₅)═C(R₆)—*′, *—C(═S)—*′, and *—C≡C—*′, L₅ is selected from a single bond, a substituted or unsubstituted C₅-C₃₀ carbocyclic group, and a substituted or unsubstituted C₁-C₃₀ heterocyclic group, b5 is selected from 1 to 3, wherein, when b5 is two or more, two or more groups L₅ are identical to or different from each other, R₅ and R₆ are optionally linked via a first linking group to form a substituted or unsubstituted C₅-C₃₀ carbocyclic group or a substituted or unsubstituted C₁-C₃₀ heterocyclic group, n1 to n3 are each independently 0, 1, 2, or 3, wherein, when n1 is zero, *-(T)_(n1)-*′ is a single bond, when n2 is zero, *-(T₂)_(n2)-*′ is a single bond, and when n3 is zero, *-(T₃)_(n3)-*′ is a single bond, X₁₁ is N or C(R₁₁), X₁₂ is N or C(R₁₂), X₁₃ is N or C(R₁₃), X₁₄ is N or C(R₁₄), X₅ is N or C(R₁₅), X₁₆ is N or C(R₁₆), X₁₇ is N or C(R₁₇), X₂₁ is N or C(R₂₁), X₂₂ is N or C(R₂₂), X₂₃ is N or C(R₂₃), X₂₄ is N or C(R₂₄), X₂₅ is N or C(R₂₅), X₂₆ is N or C(R₂₆), X₃₁ is N or C(R₃₁), X₃₂ is N or C(R₃₂), X₃₃ is N or C(R₃₃), X₃₄ is N or C(R₃₄), X₃₅ is N or C(R₃₅), X₃₆ is N or C(R₃₆), X₄₁ is N or C(R₄₁), X₄₂ is N or C(R₄₂), X₄₃ is N or C(R₄₃), X₄₄ is N or C(R₄₄), X₄₅ is N or C(R₄₅), X₄₆ is N or C(R₄₆), and X₄₇ is N or C(R₄₇), R₁, R₃ to R₆, R₁₁ to R₁₇, R₂₁ to R₂₆, R₃₁ to R₃₆, and R₄₁ to R₄₇ are each independently selected from hydrogen, deuterium, —F, —Cl, —Br, —I, —SF₅, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a substituted or unsubstituted C₁-C₆₀ alkyl group, a substituted or unsubstituted C₂-C₆₀ alkenyl group, a substituted or unsubstituted C₂-C₆₀ alkynyl group, a substituted or unsubstituted C₁-C₆₀ alkoxy group, a substituted or unsubstituted C₃-C₁₀ cycloalkyl group, a substituted or unsubstituted C₁-C₁₀ heterocycloalkyl group, a substituted or unsubstituted C₃-C₁₀ cycloalkenyl group, a substituted or unsubstituted C₁-C₁₀ heterocycloalkenyl group, a substituted or unsubstituted C₆-C₆₀ aryl group, a substituted or unsubstituted C₆-C₆₀ aryloxy group, a substituted or unsubstituted C₆-C₆₀ arylthio group, a substituted or unsubstituted C₇-C₆₀ arylalkyl group, a substituted or unsubstituted C₁-C₆₀ heteroaryl group, a substituted or unsubstituted C₁-C₆₀ heteroaryloxy group, a substituted or unsubstituted C₁-C₆₀ heteroarylthio group, a substituted or unsubstituted C₂-C₆₀ heteroarylalkyl group, a substituted or unsubstituted monovalent non-aromatic condensed polycyclic group, a substituted or unsubstituted monovalent non-aromatic condensed heteropolycyclic group, —N(Q₁)(Q₂), —Si(Q₃)(Q₄)(Q₅), —B(Q₆)(Q₇), and —P(═O)(Q₈)(Q₉), a1, a3, and a4 are each independently 0, 1, 2, 3, 4, or 5, two of groups R₁ in the number of a1 are optionally linked to form a substituted or unsubstituted C₅-C₃₀ carbocyclic group or a substituted or unsubstituted C₁-C₃₀ heterocyclic group, two of groups R₃ in the number of a3 are optionally linked to form a substituted or unsubstituted C₅-C₃₀ carbocyclic group or a substituted or unsubstituted C₁-C₃₀ heterocyclic group, two of groups R₄ in the number of a4 are optionally linked to form a substituted or unsubstituted C₅-C₃₀ carbocyclic group or a substituted or unsubstituted C₁-C₃₀ heterocyclic group, two of R₁₁ to R₁₇ are optionally linked to form a substituted or unsubstituted C₅-C₃₀ carbocyclic group or a substituted or unsubstituted C₁-C₃₀ heterocyclic group, two of R₂₁ to R₂₆ are optionally linked to form a substituted or unsubstituted C₅-C₃₀ carbocyclic group or a substituted or unsubstituted C₁-C₃₀ heterocyclic group, two of R₃₁ to R₃₆ are optionally linked to form a substituted or unsubstituted C₅-C₃₀ carbocyclic group or a substituted or unsubstituted C₁-C₃₀ heterocyclic group, two of R₄₁ to R₄₇ are optionally linked to form a substituted or unsubstituted C₅-C₃₀ carbocyclic group or a substituted or unsubstituted C₁-C₃₀ heterocyclic group, *′, *′, and *″ each indicate a binding site to a neighboring atom, at least one substituent of the substituted C₅-C₃₀ carbocyclic group, the substituted C₁-C₃₀ heterocyclic group, the substituted C₁-C₆₀ alkyl group, the substituted C₂-C₆₀ alkenyl group, the substituted C₂-C₆₀ alkynyl group, the substituted C₁-C₆₀ alkoxy group, the substituted C₃-C₁₀ cycloalkyl group, the substituted C₁-C₁₀ heterocycloalkyl group, the substituted C₃-C₁₀ cycloalkenyl group, the substituted C₁-C₁₀ heterocycloalkenyl group, the substituted C₆-C₆₀ aryl group, the substituted C₆-C₆₀ aryloxy group, the substituted C₆-C₆₀ arylthio group, the substituted C₇-C₆₀ arylalkyl group, the substituted C₁-C₆₀ heteroaryl group, the substituted C₂-C₆₀ heteroaryloxy group, the substituted C₁-C₆₀ heteroarylthio group, the substituted C₂-C₆₀ heteroarylalkyl group, the substituted monovalent non-aromatic condensed polycyclic group, and the substituted monovalent non-aromatic condensed heteropolycyclic group is selected from: deuterium, —F, Cl, —Br, —I, —CD₃, —CD₂H, —CDH₂, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl group, and a C₁-C₆₀ alkoxy group; a C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl group, and a C₁-C₆₀ alkoxy group, each substituted with at least one selected from deuterium, —F, —Cl, —Br, —I, —CD₃, —CD₂H, —CDH₂, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C₃-C₁ cycloalkyl group, a C₁-C₁₀ heterocycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀ heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio group, a C₇-C₆₀ arylalkyl group, a C₁-C₆₀ heteroaryl group, a C₁-C₆₀ heteroaryloxy group, a C₁-C₆₀ heteroarylthio group, a C₂-C₆₀ heteroarylalkyl group, a monovalent non-aromatic condensed polycyclic group, a monovalent non-aromatic condensed heteropolycyclic group, —N(Q₁₁)(Q₁₂), —Si(Q₁₃)(Q₁₄)(Q₁₅), —B(Q₁₆)(Q₁₇), and —P(═O)(Q₁₈)(Q₁₉); a C₃-C₁₀ cycloalkyl group, a C₁-C₁₀ heterocycloalkyl group, a C₃—C cycloalkenyl group, a C₁-C₁₀ heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio group, a C₇-C₆₀ arylalkyl group, a C₁-C₆₀ heteroaryl group, a C₁-C₆₀ heteroaryloxy group, a C₁-C₆₀ heteroarylthio group, a C₂-C₆₀ heteroarylalkyl group, a monovalent non-aromatic condensed polycyclic group, and a monovalent non-aromatic condensed heteropolycyclic group; a C₃-C₁₀ cycloalkyl group, a C₁-C₁₀ heterocycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀ heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio group, a C₇-C₆₀ arylalkyl group, a C₁-C₆₀ heteroaryl group, a C₁-C₆₀ heteroaryloxy group, a C₁-C₆₀ heteroarylthio group, a C₂-C₆₀ heteroarylalkyl group, a monovalent non-aromatic condensed polycyclic group, and a monovalent non-aromatic condensed heteropolycyclic group, each substituted with at least one selected from deuterium, —F, —Cl, —Br, —I, —CD₃, —CD₂H, —CDH₂, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl group, a C₁-C₆₀ alkoxy group, a C₃-C₆₀ cycloalkyl group, a C₁-C₁₀ heterocycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀ heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio group, a C₇-C₆₀ arylalkyl group, a C₁-C₆₀ heteroaryl group, a C₁-C₆₀ heteroaryloxy group, a C₁-C₆₀ heteroarylthio group, a C₂-C₆₀ heteroarylalkyl group, a monovalent non-aromatic condensed polycyclic group, a monovalent non-aromatic condensed heteropolycyclic group, —N(Q₂₁)(Q₂₂), —Si(Q₂₃)(Q₂₄)(Q₂₅), —B(Q₂₆)(Q₂₇), and —P(═O)(Q₂₈)(Q₂₉); and —N(Q₃₁)(Q₃₂), —Si(Q₃₃)(Q₃₄)(Q₃₅), —B(Q₃₆)(Q₃₇), and —P(═O)(Q₃₈)(Q₃₉), Q₁ to Q₉, Q₁₁ to Q₁₉, Q₂₁ to Q₂₉, and Q₃₁ to Q₃₉ are each independently selected from hydrogen, deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C₁-C₆₀ alkyl group, a C₂-C₆₀ alkenyl group, a C₂-C₆₀ alkynyl group, a C₁-C₆₀ alkoxy group, a C₃-C₁₀ cycloalkyl group, a C₁-C₁₀ heterocycloalkyl group, a C₃-C₁₀ cycloalkenyl group, a C₁-C₁₀ heterocycloalkenyl group, a C₆-C₆₀ aryl group, a C₆-C₆₀ aryl group substituted with at least one selected from a C₁-C₆₀ alkyl group and a C₆-C₆₀ aryl group, a C₆-C₆₀ aryloxy group, a C₆-C₆₀ arylthio group, a C₇-C₆₀ arylalkyl group, a C₁-C₆₀ heteroaryl group, a C₁-C₆₀ heteroaryloxy group, a C₁-C₆₀ heteroarylthio group, a C₂-C₆₀ heteroarylalkyl group, a monovalent non-aromatic condensed polycyclic group, and a monovalent non-aromatic condensed heteropolycyclic group, and Formula 1 satisfies at least one of Condition 1 to Condition 4: Condition 1 CY₁ in Formula 1 is a group represented by Formula CZ1, provided that at least one of X₁₁ to X₁₇ in Formula CZ1 is each independently N or C(CN), Condition 2 at least one of X₂₁ to X₂₆ in Formula 1 is each independently N or C(CN), Condition 3 CY₃ in Formula 1 is a group represented by Formula CZ3, provided that at least one of X₃₁ to X₃₆ in Formula CZ3 is each independently N or C(CN), and Condition 4 CY₄ in Formula 1 is a group represented by Formula CZ4, provided that at least one of X₄₁ to X₄₇ in Formula CZ4 is each independently N or C(CN).
 2. The organometallic compound of claim 1, wherein M is Pt or Pd.
 3. The organometallic compound of claim 1, wherein i) X₁ and X₄ are each N, X₂ and X₃ are each C, a bond between X₁ and M and a bond between X₄ and M are each a coordinate bond, and a bond between X₂ and M and a bond between X₃ and M are each a covalent bond; ii) X₁ and X₃ are each N, X₂ and X₄ are each C, a bond between X₁ and M and a bond between X₃ and M are each a coordinate bond, and a bond between X₂ and M and a bond between X₄ and M are each a covalent bond; or iii) X₃ and X₄ are each N, X₁ and X₂ are each C, a bond between X₃ and M and a bond between X₄ and M are each a coordinate bond, and a bond between X₁ and M and a bond between X₂ and M are each a covalent bond.
 4. The organometallic compound of claim 1, wherein CY₁, CY₃, and CY₄ are each independently selected from a benzene group, a naphthalene group, an anthracene group, a phenanthrene group, a triphenylene group, a pyrene group, a chrysene group, a cyclopentadiene group, a 1,2,3,4-tetrahydronaphthalene group, a pyrrole group, a thiophene group, a furan group, an indole group, an iso-indole group, a benzoborole group, a benzophosphole group, an indene group, a benzosilole group, a benzogermole group, a benzothiophene group, a benzoselenophene group, a benzofuran group, a carbazole group, a dibenzoborole group, a dibenzophosphole group, a fluorene group, a dibenzosilole group, a dibenzogermole group, a dibenzothiophene group, a dibenzoselenophene group, a dibenzofuran group, a dibenzothiophene 5-oxide group, a 9H-fluorene-9-on group, a dibenzothiophene 5,5-dioxide group, an azacarbazole group, an azadibenzoborole group, an azadibenzophosphole group, an azafluorene group, an azadibenzosilole group, an azadibenzogermole group, an azadibenzothiophene group, an azadibenzoselenophene group, an azadibenzofuran group, an azadibenzothiophene 5-oxide group, an aza-9H-fluorene-9-on group, an azadibenzothiophene 5,5-dioxide group, a pyridine group, a pyrimidine group, a pyrazine group, a pyridazine group, a triazine group, a quinoline group, an isoquinoline group, a quinoxaline group, a quinazoline group, a phenanthroline group, a pyrazole group, an imidazole group, a triazole group, a tetrazole group, an oxazole group, an isoxazole group, a thiazole group, an isothiazole group, an oxadiazole group, a thiadiazole group, a benzopyrazole group, a benzimidazole group, a benzoxazole group, a benzothiazole group, a benzoxadiazole group, a benzothiadiazole group, a 5,6,7,8-tetrahydroisoquinoline group, and a 5,6,7,8-tetrahydroquinoline group; CY₁ is a group represented by Formula CZ1; CY₃ is a group represented by Formula CZ3; or CY₄ is a group represented by Formula CZ4.
 5. The organometallic compound of claim 1, wherein, in Formula 1, a moiety represented by

and a moiety represented by

are identical to each other; a moiety represented by

and a moiety represented by

as are identical to each other; a moiety represented by

and a moiety represented by

are identical to each other; a moiety represented by

and a moiety represented by

are identical to each other; or a moiety represented by

a moiety represented by

a moiety represented by

and a moiety represented by

are different from one another.
 6. The organometallic compound of claim 1, wherein the organometallic compound has a symmetrical structure with respect to an axis connecting M and T₂ in Formula
 1. 7. The organometallic compound of claim 1, wherein T₁ to T₃ are each independently *—N[(L₅)_(b5)-(R₅)]—*′, *—B(R₅)—*′, *—C(R₅)(R₆)—*′, *—Si(R₅)(R₆)—*′, *—S—*′, or *—O—*′, and the sum of n1, n2, and n3 is 1 or
 2. 8. The organometallic compound of claim 1, wherein R₁, R₃ to R₆, R₁₁ to R₁₇, R₂₁ to R₂₆, R₃₁ to R₃₆, and R₄₁ to R₄₇ are each independently selected from: hydrogen, deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, —SF₅, C₁-C₂₀ alkyl group, and a C₁-C₂₀ alkoxy group; a C₁-C₂₀ alkyl group and a C₁-C₂₀ alkoxy group, each substituted with at least one selected from deuterium, —F, —Cl, —Br, —I, —CD₃, —CD₂H, —CDH₂, —CF₃, —CF₂H, —CFH₂, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C₁-C₁₀ alkyl group, a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a cyclooctyl group, an adamantanyl group, a norbornanyl group, a norbornenyl group, a cyclopentenyl group, a cyclohexenyl group, a cycloheptenyl group, a phenyl group, a naphthyl group, a pyridinyl group, and a pyrimidinyl group; a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a cyclooctyl group, an adamantanyl group, a norbornanyl group, a norbornenyl group, a cyclopentenyl group, a cyclohexenyl group, a cycloheptenyl group, a phenyl group, a naphthyl group, a fluorenyl group, a phenanthrenyl group, an anthracenyl group, a fluoranthenyl group, a triphenylenyl group, a pyrenyl group, a chrysenyl group, a pyrrolyl group, a thiophenyl group, a furanyl group, an imidazolyl group, a pyrazolyl group, a thiazolyl group, an isothiazolyl group, an oxazolyl group, an isoxazolyl group, a pyridinyl group, a pyrazinyl group, a pyrimidinyl group, a pyridazinyl group, an isoindolyl group, an indolyl group, an indazolyl group, a purinyl group, a quinolinyl group, an isoquinolinyl group, a benzoquinolinyl group, a quinoxalinyl group, a quinazolinyl group, a cinnolinyl group, a carbazolyl group, a phenanthrolinyl group, a benzimidazolyl group, a benzofuranyl group, a benzothiophenyl group, an isobenzothiazolyl group, a benzoxazolyl group, an isobenzoxazolyl group, a triazolyl group, a tetrazolyl group, an oxadiazolyl group, a triazinyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a benzocarbazolyl group, a dibenzocarbazolyl group, an imidazopyridinyl group, and an imidazopyrimidinyl group; a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a cyclooctyl group, an adamantanyl group, a norbornanyl group, a norbornenyl group, a cyclopentenyl group, a cyclohexenyl group, a cycloheptenyl group, a phenyl group, a naphthyl group, a fluorenyl group, a phenanthrenyl group, an anthracenyl group, a fluoranthenyl group, a triphenylenyl group, a pyrenyl group, a chrysenyl group, a pyrrolyl group, a thiophenyl group, a furanyl group, an imidazolyl group, a pyrazolyl group, a thiazolyl group, an isothiazolyl group, an oxazolyl group, an isoxazolyl group, a pyridinyl group, a pyrazinyl group, a pyrimidinyl group, a pyridazinyl group, an isoindolyl group, an indolyl group, an indazolyl group, a purinyl group, a quinolinyl group, an isoquinolinyl group, a benzoquinolinyl group, a quinoxalinyl group, a quinazolinyl group, a cinnolinyl group, a carbazolyl group, a phenanthrolinyl group, a benzimidazolyl group, a benzofuranyl group, a benzothiophenyl group, an isobenzothiazolyl group, a benzoxazolyl group, an isobenzoxazolyl group, a triazolyl group, a tetrazolyl group, an oxadiazolyl group, a triazinyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a benzocarbazolyl group, a dibenzocarbazolyl group, an imidazopyridinyl group, and an imidazopyrimidinyl group, each substituted with at least one selected from deuterium, —F, —Cl, —Br, —I, —CD₃, —CD₂H, —CDH₂, —CF₃, —CF₂H, —CFH₂, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C₁-C₂₀ alkyl group, a C₁-C₂₀ alkoxy group, a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a cyclooctyl group, an adamantanyl group, a norbornanyl group, a norbornenyl group, a cyclopentenyl group, a cyclohexenyl group, a cycloheptenyl group, a phenyl group, a naphthyl group, a fluorenyl group, a phenanthrenyl group, an anthracenyl group, a fluoranthenyl group, a triphenylenyl group, a pyrenyl group, a chrysenyl group, a pyrrolyl group, a thiophenyl group, a furanyl group, an imidazolyl group, a pyrazolyl group, a thiazolyl group, an isothiazolyl group, an oxazolyl group, an isoxazolyl group, a pyridinyl group, a pyrazinyl group, a pyrimidinyl group, a pyridazinyl group, an isoindolyl group, an indolyl group, an indazolyl group, a purinyl group, a quinolinyl group, an isoquinolinyl group, a benzoquinolinyl group, a quinoxalinyl group, a quinazolinyl group, a cinnolinyl group, a carbazolyl group, a phenanthrolinyl group, a benzimidazolyl group, a benzofuranyl group, a benzothiophenyl group, an isobenzothiazolyl group, a benzoxazolyl group, an isobenzoxazolyl group, a triazolyl group, a tetrazolyl group, an oxadiazolyl group, a triazinyl group, a dibenzofuranyl group, a dibenzothiophenyl group, a benzocarbazolyl group, a dibenzocarbazolyl group, an imidazopyridinyl group, and an imidazopyrimidinyl group; and —N(Q₁)(Q₂), —Si(Q₃)(Q₄)(Q₅), —B(Q₆)(Q₇), and —P(═O)(Q₈)(Q₉), and Q₁ to Q₉ are each independently selected from: —CH₃, —CD₃, —CD₂H, —CDH₂, —CH₂CH₃, —CH₂CD₃, —CH₂CD₂H, —CH₂CDH₂, —CHDCH₃, —CHDCD₂H, —CHDCDH₂, —CHDCD₃, —CD₂CD₃, —CD₂CD₂H, and —CD₂CDH₂; an n-propyl group, an iso-propyl group, an n-butyl group, an iso-butyl group, a sec-butyl group, a tert-butyl group, an n-pentyl group, an iso-pentyl group, a sec-pentyl group, a tert-pentyl group, a phenyl group, and a naphthyl group; and an n-propyl group, an iso-propyl group, an n-butyl group, an iso-butyl group, a sec-butyl group, a tert-butyl group, an n-pentyl group, an iso-pentyl group, a sec-pentyl group, a tert-pentyl group, a phenyl group, and a naphthyl group, each substituted with at least one selected from deuterium, a C₁-C₁₀ alkyl group, and a phenyl group.
 9. The organometallic compound of claim 1, wherein R₁, R₃ to R₆, R₁₁ to R₁₇, R₂₁ to R₂₆, R₃₁ to R₃₆, and R₄₁ to R₄₇ are each independently hydrogen, deuterium, —F, a cyano group, a nitro group, —SF₅, —CH₃, —CD₃, —CD₂H, —CDH₂, —CF₃, —CF₂H, —CFH₂, groups represented by Formulae 9-1 to 9-19, groups represented by Formulae 10-1 to 10-139, and —Si(Q₃)(Q₄)(Q₅):

wherein, in Formulae 9-1 to 9-19 and 10-1 to 10-139, “Ph” indicates a phenyl group, “TMS” indicates a trimethylsilyl group, and * indicates a binding site to a neighboring atom.
 10. The organometallic compound of claim 1, wherein a moiety represented by Formula 1

is selected from groups represented by Formulae CY1-1 to CY1-39 and CZ1-1 to CZ1-8:

wherein, in Formulae CY1-1 to CY1-39 and CZ1-1 to CZ1-8, X₁ and R₁ are each independently the same as described in claim 1, X₁₈ is N or C(R₁₈), X₁₉ is O, S, N[(L₁₉)_(b19)-(R₁₉)], or C(R_(19a))(R_(19b)), R₁₁ to R₁₈ are each independently the same as described in connection with R₁ in claim 1, L₁₉ and b19 are each independently the same as described in connection with L₅ and b5 in claim 1, R₁₉, R_(19a), and R_(19b) are each independently the same as described in connection with R₅ in claim 1, X₁₁ to X₁₇ are each N or C(CN), a15 is an integer from 0 to 5, a14 is an integer from 0 to 4, a13 is an integer from 0 to 3, a12 is an integer from 0 to 2, and and *′ each indicate a binding site to a neighboring atom.
 11. The organometallic compound of claim 1, wherein a moiety represented by

in Formula 1 is selected from groups represented by Formulae CZ2-1 to CZ2-7:

wherein, in Formulae CZ2-1 to CZ2-7, X₂ and R₂₁ to R₂₆ are each independently the same as described in claim 1, X₂₁ to X₂₆ are each N or C(CN), and *′, and *″ each indicate a binding site to a neighboring atom.
 12. The organometallic compound of claim 1, wherein a moiety represented by

in Formula 1 is selected from groups represented by Formulae CY3-1 to CY3-27 and CZ3-1 to CZ3-7:

wherein, in Formulae CY3-1 to CY3-27 and CZ3-1 to CZ3-7, X₃ and R₃ are each independently the same as described in claim 1, X₃₈ is N or C(R₃₈), X₃₉ is O, S, N[(L₃₉)_(b39)-(R₃₉)], or C(R_(39a))(R_(39b)), R₃₁ to R₃₈ are each independently the same as described in connection with R₁ in claim 1, L₃₉ and b39 are each independently the same as described in connection with L₅ and b5 in claim 1, R₃₉, R_(39a), and R_(39b) are each independently the same as described in connection with R₅ in claim 1, X₃₁ to X₃₆ are each N or C(CN), a34 is an integer from 0 to 4, a33 is an integer from 0 to 3, a32 is an integer from 0 to 2, and *, *′, and *″ each indicate a binding site to a neighboring atom.
 13. The organometallic compound of claim 1, wherein a moiety represented by

in Formula 1 is selected from groups represented by Formulae CY4-1 to CY3-39 and CZ4-1 to CZ4-8:

wherein, in Formulae CY4-1 to CY4-39 and CZ4-1 to CZ4-8, X₄ and R₄ are each independently the same as described in claim 1, X₄₈ is N or C(R₄₈), X₄₉ is O, S, N[(L₄₉)_(b49)-(R₄₉)], or C(R_(49a))(R_(49b)), R₄₁ to R₄₈ are each independently the same as described in connection with R₁ in claim 1, L₄₉ and b49 are each independently the same as described in connection with L₅ and b5 in claim 1, R₄₉, R_(49a), and R_(49b) are each independently the same as described in connection with R₅ in claim 1, X₄₁ to X₄₇ are each N or C(CN), a45 is an integer from 0 to 5, a44 is an integer from 0 to 4, a43 is an integer from 0 to 3, a42 is an integer from 0 to 2, and and *′ each indicate a binding site to a neighboring atom.
 14. The organometallic compound of claim 1, wherein the organometallic compound satisfies at least one of Condition 1-1 to Condition 4-1: Condition 1-1 a moiety represented by

in Formula 1 is selected from groups represented by Formulae CZ1-1 to CZ1-7, Condition 2-1 a moiety represented by

in Formula 1 is selected from groups represented by Formulae CZ2-1 to CZ2-6, Condition 3-1 a moiety represented by

in Formula 1 is selected from groups represented by Formulae CZ3-1 to CZ3-6, and Condition 4-1 a moiety represented by

in Formula 1 is selected from groups represented by Formulae CZ4-1 to CZ4-7:

wherein, in Formulae CZ1-1 to CZ1-7, CZ2-1 to CZ2-6, CZ3-1 to CZ3-6, and CZ4-1 to CZ4-7, X₁, X₂, X₃, X₄, R₁₁ to R₁₇, R₂₁ to R₂₆, R₃₁ to R₃₆, and R₄₁ to R₄₇ are each independently the same as described in claim 1, X₁₁ Ito X₁₇, X₂₁ to X₂₆, X₃₁ to X₃₆, and X₄₁ to X₄₇ are each independently N or C(CN), and *, *′, and *″ each indicate a binding site to a neighboring atom.
 15. The organometallic compound of claim 1, wherein the organometallic compound is selected from Compounds 1 to 136:


16. An organic light-emitting device comprising: a first electrode; a second electrode; and an organic layer disposed between the first electrode and the second electrode, wherein the organic layer comprises an emission layer and at least one organometallic compound of claim
 1. 17. The organic light-emitting device of claim 16, wherein the first electrode is an anode, the second electrode is a cathode, the organic layer further comprises a hole transport region disposed between the first electrode and the emission layer and an electron transport region disposed between the emission layer and the second electrode, the hole transport region comprises a hole injection layer, a hole transport layer, an electron blocking layer, or any combination thereof, and the electron transport region comprises a hole blocking layer, an electron transport layer, an electron injection layer, or any combination thereof.
 18. The organic light-emitting device of claim 16, wherein the emission layer comprises the organometallic compound.
 19. The organic light-emitting device of claim 18, wherein the emission layer further comprises a host, and an amount of the host in the emission layer is larger than an amount of the organometallic compound in the emission layer.
 20. A diagnostic composition comprising at least one organometallic compound of claim
 1. 